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rs184474885

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs184474885(A;A)
Make rs184474885(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position130137123
GeneAIFM1
is asnp
is mentioned by
dbSNPrs184474885
ebirs184474885
HLIrs184474885
Exacrs184474885
Varsomers184474885
Maprs184474885
PheGenIrs184474885
hapmaprs184474885
1000 genomesrs184474885
hgdprs184474885
ensemblrs184474885
gopubmedrs184474885
geneviewrs184474885
scholarrs184474885
googlers184474885
pharmgkbrs184474885
gwascentralrs184474885
openSNPrs184474885
23andMers184474885
23andMe allrs184474885
SNP Nexus

SNPshotrs184474885
SNPdbers184474885
MSV3drs184474885
GWAS Ctlgrs184474885
Max Magnitude0
ClinVar
Risk rs184474885(A;A)
Alt rs184474885(A;A)
Reference rs184474885(G;G)
Significance Other
Disease Deafness
Variation info
Gene AIFM1
CLNDBN Deafness, X-linked 5
Reversed 0
HGVS NC_000023.10:g.129271098G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149862.1,