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rs863223898

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223898(G;G)
Make rs863223898(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position130136166
GeneAIFM1
is asnp
is mentioned by
dbSNPrs863223898
ebirs863223898
HLIrs863223898
Exacrs863223898
Varsomers863223898
Maprs863223898
PheGenIrs863223898
hapmaprs863223898
1000 genomesrs863223898
hgdprs863223898
ensemblrs863223898
gopubmedrs863223898
geneviewrs863223898
scholarrs863223898
googlers863223898
pharmgkbrs863223898
gwascentralrs863223898
openSNPrs863223898
23andMers863223898
23andMe allrs863223898
SNP Nexus

SNPshotrs863223898
SNPdbers863223898
MSV3drs863223898
GWAS Ctlgrs863223898
Max Magnitude0
ClinVar
Risk rs863223898(G;G)
Alt rs863223898(G;G)
Reference rs863223898(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AIFM1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.129270141A>C
CLNSRC
CLNACC RCV000197930.2,