Know any genomes at Twitter support? Contact us if you can help get their attention.

Rs104894922

From SNPedia
Jump to: navigation, search

Orientationplus
is asnp
is mentioned by
dbSNPrs104894922
PheGenIrs104894922
nextbiors104894922
hapmaprs104894922
1000 genomesrs104894922
hgdprs104894922
ensemblrs104894922
gopubmedrs104894922
geneviewrs104894922
scholarrs104894922
googlers104894922
pharmgkbrs104894922
gwascentralrs104894922
openSNPrs104894922
23andMers104894922
23andMe allrs104894922
SNP Nexus

SNPshotrs104894922
SNPdbers104894922
MSV3drs104894922
GenePOU3F4
ChromosomeX
Orientationplus
Position83509324
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894922(A;G)
Make rs104894922(G;G)
OMIM300039
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894922(G;G)
Alt rs104894922(G;G)
Reference rs104894922(A;A)
Significance 5
Disease Deafness
ClinVar info
Gene POU3F4
CLNDBN Deafness, X-linked 2
Reversed 0
CLNHGVS NC_000023.10:g.82764332A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012446.23