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rs1064795536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome12
Position109784373
GeneTRPV4
is asnp
is mentioned by
dbSNPrs1064795536
dbSNP (old)rs1064795536
ClinGenrs1064795536
ebirs1064795536
HLIrs1064795536
Exacrs1064795536
Gnomadrs1064795536
Varsomers1064795536
Maprs1064795536
PheGenIrs1064795536
Biobankrs1064795536
1000 genomesrs1064795536
hgdprs1064795536
ensemblrs1064795536
gopubmedrs1064795536
geneviewrs1064795536
scholarrs1064795536
googlers1064795536
pharmgkbrs1064795536
gwascentralrs1064795536
openSNPrs1064795536
23andMers1064795536
23andMe allrs1064795536
SNPshotrs1064795536
SNPdbers1064795536
MSV3drs1064795536
GWAS Ctlgrs1064795536
Max Magnitude0
ClinVar
Risk rs1064795536(G;G)
Alt rs1064795536(G;G)
Reference Rs1064795536(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRPV4
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.110222178T>C
CLNSRC
CLNACC RCV000478473.1,