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rs794729174

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729174(C;T)
Make rs794729174(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154419608
GeneTAZ
is asnp
is mentioned by
dbSNPrs794729174
ebirs794729174
HLIrs794729174
Exacrs794729174
Varsomers794729174
Maprs794729174
PheGenIrs794729174
hapmaprs794729174
1000 genomesrs794729174
hgdprs794729174
ensemblrs794729174
gopubmedrs794729174
geneviewrs794729174
scholarrs794729174
googlers794729174
pharmgkbrs794729174
gwascentralrs794729174
openSNPrs794729174
23andMers794729174
23andMe allrs794729174
SNP Nexus

SNPshotrs794729174
SNPdbers794729174
MSV3drs794729174
GWAS Ctlgrs794729174
Max Magnitude0
ClinVar
Risk rs794729174(T;T)
Alt rs794729174(T;T)
Reference rs794729174(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TAZ
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153647947C>T
CLNSRC
CLNACC RCV000183915.1,