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rs876661112

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661112(A;G)
Make rs876661112(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154420901
GeneTAZ
is asnp
is mentioned by
dbSNPrs876661112
ebirs876661112
HLIrs876661112
Exacrs876661112
Varsomers876661112
Maprs876661112
PheGenIrs876661112
hapmaprs876661112
1000 genomesrs876661112
hgdprs876661112
ensemblrs876661112
gopubmedrs876661112
geneviewrs876661112
scholarrs876661112
googlers876661112
pharmgkbrs876661112
gwascentralrs876661112
openSNPrs876661112
23andMers876661112
23andMe allrs876661112
SNP Nexus

SNPshotrs876661112
SNPdbers876661112
MSV3drs876661112
GWAS Ctlgrs876661112
Max Magnitude0
ClinVar
Risk rs876661112(G;G)
Alt rs876661112(G;G)
Reference rs876661112(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TAZ
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.153649240A>G
CLNSRC
CLNACC RCV000216377.1,