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rs863223696

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223696(A;A)
Make rs863223696(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71132100
GeneMED12
is asnp
is mentioned by
dbSNPrs863223696
ebirs863223696
HLIrs863223696
Exacrs863223696
Varsomers863223696
Maprs863223696
PheGenIrs863223696
hapmaprs863223696
1000 genomesrs863223696
hgdprs863223696
ensemblrs863223696
gopubmedrs863223696
geneviewrs863223696
scholarrs863223696
googlers863223696
pharmgkbrs863223696
gwascentralrs863223696
openSNPrs863223696
23andMers863223696
23andMe allrs863223696
SNP Nexus

SNPshotrs863223696
SNPdbers863223696
MSV3drs863223696
GWAS Ctlgrs863223696
Max Magnitude0
ClinVar
Risk rs863223696(A;A)
Alt rs863223696(A;A)
Reference rs863223696(G;G)
Significance Pathogenic
Disease not provided FG syndrome
Variation info
Gene MED12
CLNDBN not provided FG syndrome
Reversed 0
HGVS NC_000023.10:g.70351950G>A
CLNSRC
CLNACC RCV000195723.2, RCV000239402.1,