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

rs863223711

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223711(C;T)
Make rs863223711(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71118818
GeneMED12
is asnp
is mentioned by
dbSNPrs863223711
ebirs863223711
HLIrs863223711
Exacrs863223711
Varsomers863223711
Maprs863223711
PheGenIrs863223711
hapmaprs863223711
1000 genomesrs863223711
hgdprs863223711
ensemblrs863223711
gopubmedrs863223711
geneviewrs863223711
scholarrs863223711
googlers863223711
pharmgkbrs863223711
gwascentralrs863223711
openSNPrs863223711
23andMers863223711
23andMe allrs863223711
SNP Nexus

SNPshotrs863223711
SNPdbers863223711
MSV3drs863223711
GWAS Ctlgrs863223711
Max Magnitude0
ClinVar
Risk rs863223711(T;T)
Alt rs863223711(T;T)
Reference rs863223711(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED12
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70338668C>T
CLNSRC
CLNACC RCV000200077.1,