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rs876661124

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661124(C;G)
Make rs876661124(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position109814507
GeneTRPV4
is asnp
is mentioned by
dbSNPrs876661124
ebirs876661124
HLIrs876661124
Exacrs876661124
Varsomers876661124
Maprs876661124
PheGenIrs876661124
hapmaprs876661124
1000 genomesrs876661124
hgdprs876661124
ensemblrs876661124
gopubmedrs876661124
geneviewrs876661124
scholarrs876661124
googlers876661124
pharmgkbrs876661124
gwascentralrs876661124
openSNPrs876661124
23andMers876661124
23andMe allrs876661124
SNP Nexus

SNPshotrs876661124
SNPdbers876661124
MSV3drs876661124
GWAS Ctlgrs876661124
Max Magnitude0
ClinVar
Risk rs876661124(G;G)
Alt rs876661124(G;G)
Reference rs876661124(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRPV4
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.110252312G>C
CLNSRC
CLNACC RCV000221001.1,