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rs863225431

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225431(A;A)
Make rs863225431(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position130133409
GeneAIFM1
is asnp
is mentioned by
dbSNPrs863225431
ebirs863225431
HLIrs863225431
Exacrs863225431
Varsomers863225431
Maprs863225431
PheGenIrs863225431
hapmaprs863225431
1000 genomesrs863225431
hgdprs863225431
ensemblrs863225431
gopubmedrs863225431
geneviewrs863225431
scholarrs863225431
googlers863225431
pharmgkbrs863225431
gwascentralrs863225431
openSNPrs863225431
23andMers863225431
23andMe allrs863225431
SNP Nexus

SNPshotrs863225431
SNPdbers863225431
MSV3drs863225431
GWAS Ctlgrs863225431
Max Magnitude0
ClinVar
Risk rs863225431(A;A)
Alt rs863225431(A;A)
Reference rs863225431(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129267384C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202363.1,