Rs104894924

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894924(C;G)
Make rs104894924(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position83509291
GenePOU3F4
is asnp
is mentioned by
dbSNPrs104894924
Exacrs104894924
PheGenIrs104894924
nextbiors104894924
hapmaprs104894924
1000 genomesrs104894924
hgdprs104894924
ensemblrs104894924
gopubmedrs104894924
geneviewrs104894924
scholarrs104894924
googlers104894924
pharmgkbrs104894924
gwascentralrs104894924
openSNPrs104894924
23andMers104894924
23andMe allrs104894924
SNP Nexus

SNPshotrs104894924
SNPdbers104894924
MSV3drs104894924
Max Magnitude0
OMIM300039
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104894924(G;G)
Alt rs104894924(G;G)
Reference rs104894924(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene POU3F4
CLNDBN Deafness, X-linked 2
Reversed 0
HGVS NC_000023.10:g.82764299C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012450.23,