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rs1064795696

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position109798822
GeneTRPV4
is asnp
is mentioned by
dbSNPrs1064795696
dbSNP (old)rs1064795696
ClinGenrs1064795696
ebirs1064795696
HLIrs1064795696
Exacrs1064795696
Gnomadrs1064795696
Varsomers1064795696
Maprs1064795696
PheGenIrs1064795696
Biobankrs1064795696
1000 genomesrs1064795696
hgdprs1064795696
ensemblrs1064795696
gopubmedrs1064795696
geneviewrs1064795696
scholarrs1064795696
googlers1064795696
pharmgkbrs1064795696
gwascentralrs1064795696
openSNPrs1064795696
23andMers1064795696
23andMe allrs1064795696
SNPshotrs1064795696
SNPdbers1064795696
MSV3drs1064795696
GWAS Ctlgrs1064795696
Max Magnitude0
ClinVar
Risk rs1064795696(A;A)
Alt rs1064795696(A;A)
Reference Rs1064795696(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRPV4
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.110236627C>T
CLNSRC
CLNACC RCV000486469.1,