Rs104894920

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894920(A;T)
Make rs104894920(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position83508928
GenePOU3F4
is asnp
is mentioned by
dbSNPrs104894920
PheGenIrs104894920
nextbiors104894920
hapmaprs104894920
1000 genomesrs104894920
hgdprs104894920
ensemblrs104894920
gopubmedrs104894920
geneviewrs104894920
scholarrs104894920
googlers104894920
pharmgkbrs104894920
gwascentralrs104894920
openSNPrs104894920
23andMers104894920
23andMe allrs104894920
SNP Nexus

SNPshotrs104894920
SNPdbers104894920
MSV3drs104894920
Max Magnitude0
OMIM300039
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894920(T;T)
Alt rs104894920(T;T)
Reference rs104894920(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene POU3F4
CLNDBN Deafness, X-linked 2
Reversed 0
HGVS NC_000023.10:g.82763936A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012444.13,