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rs724160022

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs724160022(C;T)
Make rs724160022(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130133337
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160022
ebirs724160022
HLIrs724160022
Exacrs724160022
Varsomers724160022
Maprs724160022
PheGenIrs724160022
hapmaprs724160022
1000 genomesrs724160022
hgdprs724160022
ensemblrs724160022
gopubmedrs724160022
geneviewrs724160022
scholarrs724160022
googlers724160022
pharmgkbrs724160022
gwascentralrs724160022
openSNPrs724160022
23andMers724160022
23andMe allrs724160022
SNP Nexus

SNPshotrs724160022
SNPdbers724160022
MSV3drs724160022
GWAS Ctlgrs724160022
Max Magnitude0
ClinVar
Risk rs724160022(T;T)
Alt rs724160022(T;T)
Reference rs724160022(C;C)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129267312G>A
CLNSRC
CLNACC RCV000149866.1,