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rs879255526

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255526(A;G)
Make rs879255526(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71127978
GeneMED12
is asnp
is mentioned by
dbSNPrs879255526
ebirs879255526
HLIrs879255526
Exacrs879255526
Varsomers879255526
Maprs879255526
PheGenIrs879255526
hapmaprs879255526
1000 genomesrs879255526
hgdprs879255526
ensemblrs879255526
gopubmedrs879255526
geneviewrs879255526
scholarrs879255526
googlers879255526
pharmgkbrs879255526
gwascentralrs879255526
openSNPrs879255526
23andMers879255526
23andMe allrs879255526
SNP Nexus

SNPshotrs879255526
SNPdbers879255526
MSV3drs879255526
GWAS Ctlgrs879255526
Max Magnitude0
ClinVar
Risk rs879255526(G;G)
Alt rs879255526(G;G)
Reference rs879255526(A;A)
Significance Pathogenic
Disease FG syndrome
Variation info
Gene MED12
CLNDBN FG syndrome
Reversed 0
HGVS NC_000023.10:g.70347828A>G
CLNSRC
CLNACC RCV000239400.1,