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rs267607140

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607140(A;A)
Make rs267607140(A;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position31028454
GeneTRPM1
is asnp
is mentioned by
dbSNPrs267607140
ebirs267607140
HLIrs267607140
Exacrs267607140
Varsomers267607140
Maprs267607140
PheGenIrs267607140
hapmaprs267607140
1000 genomesrs267607140
hgdprs267607140
ensemblrs267607140
gopubmedrs267607140
geneviewrs267607140
scholarrs267607140
googlers267607140
pharmgkbrs267607140
gwascentralrs267607140
openSNPrs267607140
23andMers267607140
23andMe allrs267607140
SNP Nexus

SNPshotrs267607140
SNPdbers267607140
MSV3drs267607140
GWAS Ctlgrs267607140
Max Magnitude0
ClinVar
Risk rs267607140(A;A)
Alt rs267607140(A;A)
Reference rs267607140(T;T)
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.31320657A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006603.4,