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rs794729172

From SNPedia

Orientationplus
Make rs794729172(A;A)
Make rs794729172(A;CG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154420705
GeneTAZ
is asnp
is mentioned by
dbSNPrs794729172
ebirs794729172
HLIrs794729172
Exacrs794729172
Varsomers794729172
Maprs794729172
PheGenIrs794729172
hapmaprs794729172
1000 genomesrs794729172
hgdprs794729172
ensemblrs794729172
gopubmedrs794729172
geneviewrs794729172
scholarrs794729172
googlers794729172
pharmgkbrs794729172
gwascentralrs794729172
openSNPrs794729172
23andMers794729172
23andMe allrs794729172
SNP Nexus

SNPshotrs794729172
SNPdbers794729172
MSV3drs794729172
GWAS Ctlgrs794729172
Max Magnitude
ClinVar
Risk rs794729172(A;A)
Alt rs794729172(A;A)
Reference rs794729172(CG;CG)
Significance Pathogenic
Disease not provided
Variation info
Gene TAZ
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153649044_153649045delCGinsA
CLNSRC
CLNACC RCV000183913.1,