Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606974

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606974(-;-)
Make rs267606974(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position83509219
GenePOU3F4
is asnp
is mentioned by
dbSNPrs267606974
ebirs267606974
HLIrs267606974
Exacrs267606974
Varsomers267606974
Maprs267606974
PheGenIrs267606974
hapmaprs267606974
1000 genomesrs267606974
hgdprs267606974
ensemblrs267606974
gopubmedrs267606974
geneviewrs267606974
scholarrs267606974
googlers267606974
pharmgkbrs267606974
gwascentralrs267606974
openSNPrs267606974
23andMers267606974
23andMe allrs267606974
SNP Nexus

SNPshotrs267606974
SNPdbers267606974
MSV3drs267606974
GWAS Ctlgrs267606974
Max Magnitude0
ClinVar
Risk rs267606974(;)
Alt rs267606974(;)
Reference rs267606974(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene POU3F4
CLNDBN Deafness, X-linked 2
Reversed 0
HGVS NC_000023.10:g.82764227delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000144387.3,