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rs191205969

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs191205969(A;G)
Make rs191205969(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position31068010
GeneTRPM1
is asnp
is mentioned by
dbSNPrs191205969
ebirs191205969
HLIrs191205969
Exacrs191205969
Varsomers191205969
Maprs191205969
PheGenIrs191205969
hapmaprs191205969
1000 genomesrs191205969
hgdprs191205969
ensemblrs191205969
gopubmedrs191205969
geneviewrs191205969
scholarrs191205969
googlers191205969
pharmgkbrs191205969
gwascentralrs191205969
openSNPrs191205969
23andMers191205969
23andMe allrs191205969
SNP Nexus

SNPshotrs191205969
SNPdbers191205969
MSV3drs191205969
GWAS Ctlgrs191205969
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs191205969(G;G)
Alt rs191205969(G;G)
Reference rs191205969(A;A)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene TRPM1
CLNDBN Congenital stationary night blindness, type 1C
Reversed 0
HGVS NC_000015.9:g.31360213A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006605.4,