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rs724160019

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs724160019(A;G)
Make rs724160019(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130136710
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160019
ebirs724160019
HLIrs724160019
Exacrs724160019
Varsomers724160019
Maprs724160019
PheGenIrs724160019
hapmaprs724160019
1000 genomesrs724160019
hgdprs724160019
ensemblrs724160019
gopubmedrs724160019
geneviewrs724160019
scholarrs724160019
googlers724160019
pharmgkbrs724160019
gwascentralrs724160019
openSNPrs724160019
23andMers724160019
23andMe allrs724160019
SNP Nexus

SNPshotrs724160019
SNPdbers724160019
MSV3drs724160019
GWAS Ctlgrs724160019
Max Magnitude0
ClinVar
Risk rs724160019(G;G)
Alt rs724160019(G;G)
Reference rs724160019(A;A)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129270685T>C
CLNSRC
CLNACC RCV000149863.1,