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rs724160015

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs724160015(C;T)
Make rs724160015(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130147792
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160015
ebirs724160015
HLIrs724160015
Exacrs724160015
Varsomers724160015
Maprs724160015
PheGenIrs724160015
hapmaprs724160015
1000 genomesrs724160015
hgdprs724160015
ensemblrs724160015
gopubmedrs724160015
geneviewrs724160015
scholarrs724160015
googlers724160015
pharmgkbrs724160015
gwascentralrs724160015
openSNPrs724160015
23andMers724160015
23andMe allrs724160015
SNP Nexus

SNPshotrs724160015
SNPdbers724160015
MSV3drs724160015
GWAS Ctlgrs724160015
Max Magnitude0
ClinVar
Risk rs724160015(T;T)
Alt rs724160015(T;T)
Reference rs724160015(C;C)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129281767G>A
CLNSRC
CLNACC RCV000149858.1,