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rs672601353

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs672601353(-;-)
Make rs672601353(-;G)
Make rs672601353(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position9765594
GeneGPR143
is asnp
is mentioned by
dbSNPrs672601353
ebirs672601353
HLIrs672601353
Exacrs672601353
Varsomers672601353
Maprs672601353
PheGenIrs672601353
hapmaprs672601353
1000 genomesrs672601353
hgdprs672601353
ensemblrs672601353
gopubmedrs672601353
geneviewrs672601353
scholarrs672601353
googlers672601353
pharmgkbrs672601353
gwascentralrs672601353
openSNPrs672601353
23andMers672601353
23andMe allrs672601353
SNP Nexus

SNPshotrs672601353
SNPdbers672601353
MSV3drs672601353
GWAS Ctlgrs672601353
Max Magnitude0
ClinVar
Risk rs672601353(G;G)
Alt rs672601353(G;G)
Reference rs672601353(;)
Significance Probable-Pathogenic
Disease Ocular albinism
Variation info
Gene GPR143
CLNDBN Ocular albinism, type I
Reversed 1
HGVS NC_000023.10:g.9733635dupC
CLNSRC
CLNACC RCV000149456.1,