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rs863223703

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223703(C;T)
Make rs863223703(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71127355
GeneMED12
is asnp
is mentioned by
dbSNPrs863223703
ebirs863223703
HLIrs863223703
Exacrs863223703
Varsomers863223703
Maprs863223703
PheGenIrs863223703
hapmaprs863223703
1000 genomesrs863223703
hgdprs863223703
ensemblrs863223703
gopubmedrs863223703
geneviewrs863223703
scholarrs863223703
googlers863223703
pharmgkbrs863223703
gwascentralrs863223703
openSNPrs863223703
23andMers863223703
23andMe allrs863223703
SNP Nexus

SNPshotrs863223703
SNPdbers863223703
MSV3drs863223703
GWAS Ctlgrs863223703
Max Magnitude0
ClinVar
Risk rs863223703(T;T)
Alt rs863223703(T;T)
Reference rs863223703(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MED12
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70347205C>T
CLNSRC
CLNACC RCV000198701.1,