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rs515726172

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726172(A;G)
Make rs515726172(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position109798774
GeneTRPV4
is asnp
is mentioned by
dbSNPrs515726172
ebirs515726172
HLIrs515726172
Exacrs515726172
Varsomers515726172
Maprs515726172
PheGenIrs515726172
hapmaprs515726172
1000 genomesrs515726172
hgdprs515726172
ensemblrs515726172
gopubmedrs515726172
geneviewrs515726172
scholarrs515726172
googlers515726172
pharmgkbrs515726172
gwascentralrs515726172
openSNPrs515726172
23andMers515726172
23andMe allrs515726172
SNP Nexus

SNPshotrs515726172
SNPdbers515726172
MSV3drs515726172
GWAS Ctlgrs515726172
Max Magnitude0
ClinVar
Risk rs515726172(G;G)
Alt rs515726172(G;G)
Reference rs515726172(A;A)
Significance Pathogenic
Disease Skeletal dysplasia
Variation info
Gene TRPV4
CLNDBN Skeletal dysplasia
Reversed 0
HGVS NC_000012.11:g.110236579A>G
CLNSRC
CLNACC RCV000202451.1,