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rs863223697

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223697(C;T)
Make rs863223697(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71132164
GeneMED12
is asnp
is mentioned by
dbSNPrs863223697
ebirs863223697
HLIrs863223697
Exacrs863223697
Varsomers863223697
Maprs863223697
PheGenIrs863223697
hapmaprs863223697
1000 genomesrs863223697
hgdprs863223697
ensemblrs863223697
gopubmedrs863223697
geneviewrs863223697
scholarrs863223697
googlers863223697
pharmgkbrs863223697
gwascentralrs863223697
openSNPrs863223697
23andMers863223697
23andMe allrs863223697
SNP Nexus

SNPshotrs863223697
SNPdbers863223697
MSV3drs863223697
GWAS Ctlgrs863223697
Max Magnitude0
ClinVar
Risk rs863223697(T;T)
Alt rs863223697(T;T)
Reference rs863223697(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED12
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70352014C>T
CLNSRC
CLNACC RCV000197941.1,