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rs794729167

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729167(A;A)
Make rs794729167(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154419745
GeneTAZ
is asnp
is mentioned by
dbSNPrs794729167
ebirs794729167
HLIrs794729167
Exacrs794729167
Varsomers794729167
Maprs794729167
PheGenIrs794729167
hapmaprs794729167
1000 genomesrs794729167
hgdprs794729167
ensemblrs794729167
gopubmedrs794729167
geneviewrs794729167
scholarrs794729167
googlers794729167
pharmgkbrs794729167
gwascentralrs794729167
openSNPrs794729167
23andMers794729167
23andMe allrs794729167
SNP Nexus

SNPshotrs794729167
SNPdbers794729167
MSV3drs794729167
GWAS Ctlgrs794729167
Max Magnitude0
ClinVar
Risk rs794729167(A;A)
Alt rs794729167(A;A)
Reference rs794729167(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TAZ
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153648084G>A
CLNSRC
CLNACC RCV000183908.1,