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rs863223899

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223899(A;A)
Make rs863223899(A;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position130129579
GeneAIFM1
is asnp
is mentioned by
dbSNPrs863223899
ClinGenrs863223899
ebirs863223899
HLIrs863223899
Exacrs863223899
Varsomers863223899
Maprs863223899
PheGenIrs863223899
hapmaprs863223899
1000 genomesrs863223899
hgdprs863223899
ensemblrs863223899
gopubmedrs863223899
geneviewrs863223899
scholarrs863223899
googlers863223899
pharmgkbrs863223899
gwascentralrs863223899
openSNPrs863223899
23andMers863223899
23andMe allrs863223899
SNP Nexus

SNPshotrs863223899
SNPdbers863223899
MSV3drs863223899
GWAS Ctlgrs863223899
Max Magnitude0
ClinVar
Risk rs863223899(A;A)
Alt rs863223899(A;A)
Reference Rs863223899(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AIFM1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.129263554A>T
CLNSRC
CLNACC RCV000199085.1,