Have questions? Visit https://www.reddit.com/r/SNPedia

rs794729166

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729166(G;T)
Make rs794729166(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154412130
GeneDNASE1L1, TAZ
is asnp
is mentioned by
dbSNPrs794729166
ebirs794729166
HLIrs794729166
Exacrs794729166
Varsomers794729166
Maprs794729166
PheGenIrs794729166
hapmaprs794729166
1000 genomesrs794729166
hgdprs794729166
ensemblrs794729166
gopubmedrs794729166
geneviewrs794729166
scholarrs794729166
googlers794729166
pharmgkbrs794729166
gwascentralrs794729166
openSNPrs794729166
23andMers794729166
23andMe allrs794729166
SNP Nexus

SNPshotrs794729166
SNPdbers794729166
MSV3drs794729166
GWAS Ctlgrs794729166
Max Magnitude0
ClinVar
Risk rs794729166(T;T)
Alt rs794729166(T;T)
Reference rs794729166(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TAZ DNASE1L1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153640467G>T
CLNSRC
CLNACC RCV000183906.1,