Have questions? Visit https://www.reddit.com/r/SNPedia

rs724160024

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs724160024(C;C)
Make rs724160024(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130130062
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160024
ebirs724160024
HLIrs724160024
Exacrs724160024
Varsomers724160024
Maprs724160024
PheGenIrs724160024
hapmaprs724160024
1000 genomesrs724160024
hgdprs724160024
ensemblrs724160024
gopubmedrs724160024
geneviewrs724160024
scholarrs724160024
googlers724160024
pharmgkbrs724160024
gwascentralrs724160024
openSNPrs724160024
23andMers724160024
23andMe allrs724160024
SNP Nexus

SNPshotrs724160024
SNPdbers724160024
MSV3drs724160024
GWAS Ctlgrs724160024
Max Magnitude0
ClinVar
Risk rs724160024(C;C)
Alt rs724160024(C;C)
Reference rs724160024(T;T)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129264037A>G
CLNSRC
CLNACC RCV000149868.1,