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rs724160023

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs724160023(A;A)
Make rs724160023(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130131756
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160023
ebirs724160023
HLIrs724160023
Exacrs724160023
Varsomers724160023
Maprs724160023
PheGenIrs724160023
hapmaprs724160023
1000 genomesrs724160023
hgdprs724160023
ensemblrs724160023
gopubmedrs724160023
geneviewrs724160023
scholarrs724160023
googlers724160023
pharmgkbrs724160023
gwascentralrs724160023
openSNPrs724160023
23andMers724160023
23andMe allrs724160023
SNP Nexus

SNPshotrs724160023
SNPdbers724160023
MSV3drs724160023
GWAS Ctlgrs724160023
Max Magnitude0
ClinVar
Risk rs724160023(A;A)
Alt rs724160023(A;A)
Reference rs724160023(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129265731C>T
CLNSRC
CLNACC RCV000149867.1,