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rs369742878

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369742878(A;A)
Make rs369742878(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position31031046
GeneLOC105370752, TRPM1
is asnp
is mentioned by
dbSNPrs369742878
ebirs369742878
HLIrs369742878
Exacrs369742878
Varsomers369742878
Maprs369742878
PheGenIrs369742878
hapmaprs369742878
1000 genomesrs369742878
hgdprs369742878
ensemblrs369742878
gopubmedrs369742878
geneviewrs369742878
scholarrs369742878
googlers369742878
pharmgkbrs369742878
gwascentralrs369742878
openSNPrs369742878
23andMers369742878
23andMe allrs369742878
SNP Nexus

SNPshotrs369742878
SNPdbers369742878
MSV3drs369742878
GWAS Ctlgrs369742878
Max Magnitude0
ClinVar
Risk rs369742878(A;A)
Alt rs369742878(A;A)
Reference rs369742878(G;G)
Significance Pathogenic
Disease not provided Congenital stationary night blindness
Variation info
Gene TRPM1
CLNDBN not provided Congenital stationary night blindness, type 1C
Reversed 0
HGVS NC_000015.9:g.31323249G>A
CLNSRC
CLNACC RCV000154021.2, RCV000176290.1,