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rs387907138

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907138(C;T)
Make rs387907138(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position38343192
GeneGPR179
is asnp
is mentioned by
dbSNPrs387907138
ebirs387907138
HLIrs387907138
Exacrs387907138
Varsomers387907138
Maprs387907138
PheGenIrs387907138
hapmaprs387907138
1000 genomesrs387907138
hgdprs387907138
ensemblrs387907138
gopubmedrs387907138
geneviewrs387907138
scholarrs387907138
googlers387907138
pharmgkbrs387907138
gwascentralrs387907138
openSNPrs387907138
23andMers387907138
23andMe allrs387907138
SNP Nexus

SNPshotrs387907138
SNPdbers387907138
MSV3drs387907138
GWAS Ctlgrs387907138
Max Magnitude0
ClinVar
Risk rs387907138(T;T)
Alt rs387907138(T;T)
Reference rs387907138(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene GPR179
CLNDBN Congenital stationary night blindness, type 1E
Reversed 1
HGVS NC_000017.10:g.36499075G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024201.3,