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rs879255528

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255528(G;T)
Make rs879255528(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71137821
GeneMED12
is asnp
is mentioned by
dbSNPrs879255528
ebirs879255528
HLIrs879255528
Exacrs879255528
Varsomers879255528
Maprs879255528
PheGenIrs879255528
hapmaprs879255528
1000 genomesrs879255528
hgdprs879255528
ensemblrs879255528
gopubmedrs879255528
geneviewrs879255528
scholarrs879255528
googlers879255528
pharmgkbrs879255528
gwascentralrs879255528
openSNPrs879255528
23andMers879255528
23andMe allrs879255528
SNP Nexus

SNPshotrs879255528
SNPdbers879255528
MSV3drs879255528
GWAS Ctlgrs879255528
Max Magnitude0
ClinVar
Risk rs879255528(T;T)
Alt rs879255528(T;T)
Reference rs879255528(G;G)
Significance Pathogenic
Disease FG syndrome
Variation info
Gene MED12
CLNDBN FG syndrome
Reversed 0
HGVS NC_000023.10:g.70357671G>T
CLNSRC
CLNACC RCV000239403.1,