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rs267607141

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607141(C;T)
Make rs267607141(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position31070213
GeneTRPM1
is asnp
is mentioned by
dbSNPrs267607141
ebirs267607141
HLIrs267607141
Exacrs267607141
Varsomers267607141
Maprs267607141
PheGenIrs267607141
hapmaprs267607141
1000 genomesrs267607141
hgdprs267607141
ensemblrs267607141
gopubmedrs267607141
geneviewrs267607141
scholarrs267607141
googlers267607141
pharmgkbrs267607141
gwascentralrs267607141
openSNPrs267607141
23andMers267607141
23andMe allrs267607141
SNP Nexus

SNPshotrs267607141
SNPdbers267607141
MSV3drs267607141
GWAS Ctlgrs267607141
Max Magnitude0
ClinVar
Risk rs267607141(T;T)
Alt rs267607141(T;T)
Reference rs267607141(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.31362416G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006604.3,