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rs762905361

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762905361(A;A)
Make rs762905361(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71126057
GeneMED12
is asnp
is mentioned by
dbSNPrs762905361
ebirs762905361
HLIrs762905361
Exacrs762905361
Varsomers762905361
Maprs762905361
PheGenIrs762905361
hapmaprs762905361
1000 genomesrs762905361
hgdprs762905361
ensemblrs762905361
gopubmedrs762905361
geneviewrs762905361
scholarrs762905361
googlers762905361
pharmgkbrs762905361
gwascentralrs762905361
openSNPrs762905361
23andMers762905361
23andMe allrs762905361
SNP Nexus

SNPshotrs762905361
SNPdbers762905361
MSV3drs762905361
GWAS Ctlgrs762905361
Max Magnitude0
ClinVar
Risk rs762905361(A;A)
Alt rs762905361(A;A)
Reference rs762905361(G;G)
Significance Pathogenic
Disease FG syndrome
Variation info
Gene MED12
CLNDBN FG syndrome
Reversed 0
HGVS NC_000023.10:g.70345907G>A
CLNSRC
CLNACC RCV000239397.1,