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

rs876661038

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661038(A;G)
Make rs876661038(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154419541
GeneTAZ
is asnp
is mentioned by
dbSNPrs876661038
ebirs876661038
HLIrs876661038
Exacrs876661038
Varsomers876661038
Maprs876661038
PheGenIrs876661038
hapmaprs876661038
1000 genomesrs876661038
hgdprs876661038
ensemblrs876661038
gopubmedrs876661038
geneviewrs876661038
scholarrs876661038
googlers876661038
pharmgkbrs876661038
gwascentralrs876661038
openSNPrs876661038
23andMers876661038
23andMe allrs876661038
SNP Nexus

SNPshotrs876661038
SNPdbers876661038
MSV3drs876661038
GWAS Ctlgrs876661038
Max Magnitude0
ClinVar
Risk rs876661038(G;G)
Alt rs876661038(G;G)
Reference rs876661038(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TAZ
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153647880A>G
CLNSRC
CLNACC RCV000216671.1,