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rs724160014

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs724160014(C;C)
Make rs724160014(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130165779
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160014
ebirs724160014
HLIrs724160014
Exacrs724160014
Varsomers724160014
Maprs724160014
PheGenIrs724160014
hapmaprs724160014
1000 genomesrs724160014
hgdprs724160014
ensemblrs724160014
gopubmedrs724160014
geneviewrs724160014
scholarrs724160014
googlers724160014
pharmgkbrs724160014
gwascentralrs724160014
openSNPrs724160014
23andMers724160014
23andMe allrs724160014
SNP Nexus

SNPshotrs724160014
SNPdbers724160014
MSV3drs724160014
GWAS Ctlgrs724160014
Max Magnitude0
ClinVar
Risk rs724160014(C;C)
Alt rs724160014(C;C)
Reference rs724160014(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129299753C>G
CLNSRC
CLNACC RCV000149857.1,