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rs770561064

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770561064(C;T)
Make rs770561064(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position31076919
GeneTRPM1
is asnp
is mentioned by
dbSNPrs770561064
ebirs770561064
HLIrs770561064
Exacrs770561064
Varsomers770561064
Maprs770561064
PheGenIrs770561064
hapmaprs770561064
1000 genomesrs770561064
hgdprs770561064
ensemblrs770561064
gopubmedrs770561064
geneviewrs770561064
scholarrs770561064
googlers770561064
pharmgkbrs770561064
gwascentralrs770561064
openSNPrs770561064
23andMers770561064
23andMe allrs770561064
SNP Nexus

SNPshotrs770561064
SNPdbers770561064
MSV3drs770561064
GWAS Ctlgrs770561064
Max Magnitude0
ClinVar
Risk rs770561064(T;T)
Alt rs770561064(T;T)
Reference rs770561064(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRPM1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.31369122C>T
CLNSRC
CLNACC RCV000171229.1,