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Difference between revisions of "Rs72547515"

From SNPedia
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|geno2=(C;T)
 
|geno2=(C;T)
 
|geno3=(C;C)
 
|geno3=(C;C)
|effect1=CYP1A2*16 homozygote
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|Orientation=minus
|effect2=carrier of one CYP1A2*16 allele
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|Chromosome=15
|effect3=normal
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|position=74752211
| Chromosome = 15
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|Gene=CYP1A2
}}
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|Assembly=GRCh38
 +
|GenomeBuild=38.1
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|dbSNPBuild=141
 +
|Gene_s=CYP1A2
 +
|StabilizedOrientation=minus
 +
}}[[rs72547515]], also known as 2473G>A, 5347T>C or R377Q, is a SNP in the [[CYP1A2]] gene.
  
[[rs72547515]], also known as 2473G>A, 5347T>C or R377Q, is a SNP in the [[CYP1A2]] gene.
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The [[rs72547515]](T) allele defines the CYP1A2*16 variant.
  
The [[rs72547515]](T) allele defines the CYP1A2*16 variant.
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{{on chip | 23andMe v3}}
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{{on chip | 23andMe v4}}
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{{on chip | Ancestry v2}}
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{{on chip | 23andMe v5}}
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{{on chip | Ancestry v2c}}
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{{on chip | Ancestry v2d}}

Latest revision as of 07:40, 7 December 2019

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 normal
(C;T) carrier of one CYP1A2*16 allele
(T;T) CYP1A2*16 homozygote
ReferenceGRCh38 38.1/141
Chromosome15
Position74752211
GeneCYP1A2
is asnp
is mentioned by
dbSNPrs72547515
dbSNP (classic)rs72547515
ClinGenrs72547515
ebirs72547515
HLIrs72547515
Exacrs72547515
Gnomadrs72547515
Varsomers72547515
LitVarrs72547515
Maprs72547515
PheGenIrs72547515
Biobankrs72547515
1000 genomesrs72547515
hgdprs72547515
ensemblrs72547515
geneviewrs72547515
scholarrs72547515
googlers72547515
pharmgkbrs72547515
gwascentralrs72547515
openSNPrs72547515
23andMers72547515
SNPshotrs72547515
SNPdbers72547515
MSV3drs72547515
GWAS Ctlgrs72547515
Max Magnitude0

rs72547515, also known as 2473G>A, 5347T>C or R377Q, is a SNP in the CYP1A2 gene.

The rs72547515(T) allele defines the CYP1A2*16 variant.