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rs387906862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906862(C;T)
Make rs387906862(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position31042102
GeneTRPM1
is asnp
is mentioned by
dbSNPrs387906862
ebirs387906862
HLIrs387906862
Exacrs387906862
Varsomers387906862
Maprs387906862
PheGenIrs387906862
hapmaprs387906862
1000 genomesrs387906862
hgdprs387906862
ensemblrs387906862
gopubmedrs387906862
geneviewrs387906862
scholarrs387906862
googlers387906862
pharmgkbrs387906862
gwascentralrs387906862
openSNPrs387906862
23andMers387906862
23andMe allrs387906862
SNP Nexus

SNPshotrs387906862
SNPdbers387906862
MSV3drs387906862
GWAS Ctlgrs387906862
Max Magnitude0
ClinVar
Risk rs387906862(T;T)
Alt rs387906862(T;T)
Reference rs387906862(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene TRPM1
CLNDBN Congenital stationary night blindness, type 1C
Reversed 1
HGVS NC_000015.9:g.31334305G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023310.4,