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rs724160026

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs724160026(C;C)
Make rs724160026(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130136729
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160026
ebirs724160026
HLIrs724160026
Exacrs724160026
Varsomers724160026
Maprs724160026
PheGenIrs724160026
hapmaprs724160026
1000 genomesrs724160026
hgdprs724160026
ensemblrs724160026
gopubmedrs724160026
geneviewrs724160026
scholarrs724160026
googlers724160026
pharmgkbrs724160026
gwascentralrs724160026
openSNPrs724160026
23andMers724160026
23andMe allrs724160026
SNP Nexus

SNPshotrs724160026
SNPdbers724160026
MSV3drs724160026
GWAS Ctlgrs724160026
Max Magnitude0
ClinVar
Risk rs724160026(C;C)
Alt rs724160026(C;C)
Reference rs724160026(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129270704C>G
CLNSRC
CLNACC RCV000149870.1,