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rs778390089

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778390089(-;-)
Make rs778390089(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position31026197
GeneLOC105370752, TRPM1
is asnp
is mentioned by
dbSNPrs778390089
ClinGenrs778390089
ebirs778390089
HLIrs778390089
Exacrs778390089
Varsomers778390089
Maprs778390089
PheGenIrs778390089
hapmaprs778390089
1000 genomesrs778390089
hgdprs778390089
ensemblrs778390089
gopubmedrs778390089
geneviewrs778390089
scholarrs778390089
googlers778390089
pharmgkbrs778390089
gwascentralrs778390089
openSNPrs778390089
23andMers778390089
23andMe allrs778390089
SNP Nexus

SNPshotrs778390089
SNPdbers778390089
MSV3drs778390089
GWAS Ctlgrs778390089
Max Magnitude0
ClinVar
Risk rs778390089(-;-)
Alt rs778390089(-;-)
Reference Rs778390089(C;C)
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.31318400delC
CLNSRC
CLNACC RCV000176649.1,