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rs267606975

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606975(-;-)
Make rs267606975(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position83508975
GenePOU3F4
is asnp
is mentioned by
dbSNPrs267606975
ebirs267606975
HLIrs267606975
Exacrs267606975
Varsomers267606975
Maprs267606975
PheGenIrs267606975
hapmaprs267606975
1000 genomesrs267606975
hgdprs267606975
ensemblrs267606975
gopubmedrs267606975
geneviewrs267606975
scholarrs267606975
googlers267606975
pharmgkbrs267606975
gwascentralrs267606975
openSNPrs267606975
23andMers267606975
23andMe allrs267606975
SNP Nexus

SNPshotrs267606975
SNPdbers267606975
MSV3drs267606975
GWAS Ctlgrs267606975
Max Magnitude0
ClinVar
Risk rs267606975(;)
Alt rs267606975(;)
Reference rs267606975(G;G)
Significance Untested
Disease Deafness
Variation info
Gene POU3F4
CLNDBN Deafness, X-linked 2
Reversed 0
HGVS NC_000023.10:g.82763983delG
CLNSRC ClinVar
CLNACC RCV000144386.1,