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Difference between revisions of "Rs72547515"

From SNPedia
m (moving effect2 to Rs72547515(C;T))
m (moving effect3 to Rs72547515(C;C))
Line 4: Line 4:
 
|geno2=(C;T)
 
|geno2=(C;T)
 
|geno3=(C;C)
 
|geno3=(C;C)
|effect3=normal
 
 
| Chromosome = 15
 
| Chromosome = 15
 
| position = 72831604
 
| position = 72831604

Revision as of 07:14, 8 December 2009

Orientationminus
Geno Mag Summary
(C;C) 0 normal
(C;T) carrier of one CYP1A2*16 allele
(T;T) CYP1A2*16 homozygote
Chromosome15
Position72831604
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.