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rs121965089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965089(A;A)
Make rs121965089(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position130138622
GeneAIFM1
is asnp
is mentioned by
dbSNPrs121965089
ebirs121965089
HLIrs121965089
Exacrs121965089
Varsomers121965089
Maprs121965089
PheGenIrs121965089
hapmaprs121965089
1000 genomesrs121965089
hgdprs121965089
ensemblrs121965089
gopubmedrs121965089
geneviewrs121965089
scholarrs121965089
googlers121965089
pharmgkbrs121965089
gwascentralrs121965089
openSNPrs121965089
23andMers121965089
23andMe allrs121965089
SNP Nexus

SNPshotrs121965089
SNPdbers121965089
MSV3drs121965089
GWAS Ctlgrs121965089
Max Magnitude0
ClinVar
Risk rs121965089(A;A)
Alt rs121965089(A;A)
Reference rs121965089(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129272597C>T
CLNSRC
CLNACC