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rs863223705

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223705(C;T)
Make rs863223705(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71141275
GeneMED12
is asnp
is mentioned by
dbSNPrs863223705
ebirs863223705
HLIrs863223705
Exacrs863223705
Varsomers863223705
Maprs863223705
PheGenIrs863223705
hapmaprs863223705
1000 genomesrs863223705
hgdprs863223705
ensemblrs863223705
gopubmedrs863223705
geneviewrs863223705
scholarrs863223705
googlers863223705
pharmgkbrs863223705
gwascentralrs863223705
openSNPrs863223705
23andMers863223705
23andMe allrs863223705
SNP Nexus

SNPshotrs863223705
SNPdbers863223705
MSV3drs863223705
GWAS Ctlgrs863223705
Max Magnitude0
ClinVar
Risk rs863223705(T;T)
Alt rs863223705(T;T)
Reference rs863223705(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MED12
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70361125C>T
CLNSRC
CLNACC RCV000200799.1,