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rs267607139

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607139(A;A)
Make rs267607139(A;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position31042140
GeneTRPM1
is asnp
is mentioned by
dbSNPrs267607139
ebirs267607139
HLIrs267607139
Exacrs267607139
Varsomers267607139
Maprs267607139
PheGenIrs267607139
hapmaprs267607139
1000 genomesrs267607139
hgdprs267607139
ensemblrs267607139
gopubmedrs267607139
geneviewrs267607139
scholarrs267607139
googlers267607139
pharmgkbrs267607139
gwascentralrs267607139
openSNPrs267607139
23andMers267607139
23andMe allrs267607139
SNP Nexus

SNPshotrs267607139
SNPdbers267607139
MSV3drs267607139
GWAS Ctlgrs267607139
Max Magnitude0
ClinVar
Risk rs267607139(A;A)
Alt rs267607139(A;A)
Reference rs267607139(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.31334343G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006606.3,