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rs724160020

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs724160020(C;T)
Make rs724160020(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130136086
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160020
ebirs724160020
HLIrs724160020
Exacrs724160020
Varsomers724160020
Maprs724160020
PheGenIrs724160020
hapmaprs724160020
1000 genomesrs724160020
hgdprs724160020
ensemblrs724160020
gopubmedrs724160020
geneviewrs724160020
scholarrs724160020
googlers724160020
pharmgkbrs724160020
gwascentralrs724160020
openSNPrs724160020
23andMers724160020
23andMe allrs724160020
SNP Nexus

SNPshotrs724160020
SNPdbers724160020
MSV3drs724160020
GWAS Ctlgrs724160020
Max Magnitude0
ClinVar
Risk rs724160020(T;T)
Alt rs724160020(T;T)
Reference rs724160020(C;C)
Significance Other
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129270061G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149864.1,