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rs724160021

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs724160021(A;A)
Make rs724160021(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130136085
GeneAIFM1
is asnp
is mentioned by
dbSNPrs724160021
ebirs724160021
HLIrs724160021
Exacrs724160021
Varsomers724160021
Maprs724160021
PheGenIrs724160021
hapmaprs724160021
1000 genomesrs724160021
hgdprs724160021
ensemblrs724160021
gopubmedrs724160021
geneviewrs724160021
scholarrs724160021
googlers724160021
pharmgkbrs724160021
gwascentralrs724160021
openSNPrs724160021
23andMers724160021
23andMe allrs724160021
SNP Nexus

SNPshotrs724160021
SNPdbers724160021
MSV3drs724160021
GWAS Ctlgrs724160021
Max Magnitude0
ClinVar
Risk rs724160021(A;A)
Alt rs724160021(A;A)
Reference rs724160021(G;G)
Significance Other
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 1
HGVS NC_000023.10:g.129270060C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149865.1,