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rs2733832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2733832(C;T)
Make rs2733832(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome9
Position12704725
GeneDHX29, TYRP1
is asnp
is mentioned by
dbSNPrs2733832
ClinGenrs2733832
ebirs2733832
HLIrs2733832
Exacrs2733832
Varsomers2733832
Maprs2733832
PheGenIrs2733832
hapmaprs2733832
1000 genomesrs2733832
hgdprs2733832
ensemblrs2733832
gopubmedrs2733832
geneviewrs2733832
scholarrs2733832
googlers2733832
pharmgkbrs2733832
gwascentralrs2733832
openSNPrs2733832
23andMers2733832
23andMe allrs2733832
SNP Nexus

SNPshotrs2733832
SNPdbers2733832
MSV3drs2733832
GWAS Ctlgrs2733832
GMAF0.2792
Max Magnitude0
? (C;C) (C;T) (T;T) 28

Influences appearance gnxp

[PMID 17999355OA-icon.png] A genomewide association study of skin pigmentation in a South Asian population.

[PMID 18312627OA-icon.png] Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans.


[PMID 25837821OA-icon.png] Inherited genetic variants associated with occurrence of multiple primary melanoma


ClinVar
Risk rs2733832(G;G) rs2733832(T;T)
Alt rs2733832(G;G) rs2733832(T;T)
Reference Rs2733832(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene TYRP1 LURAP1L-AS1
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.12704725C>T
CLNSRC
CLNACC RCV000251189.1,