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

rs876657719

From SNPedia

Orientationplus
Geno Mag Summary
(CAAA;CAAA) 0 common in clinvar
Make rs876657719(-;-)
Make rs876657719(-;CAAA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position83508931
GenePOU3F4
is asnp
is mentioned by
dbSNPrs876657719
ebirs876657719
HLIrs876657719
Exacrs876657719
Varsomers876657719
Maprs876657719
PheGenIrs876657719
hapmaprs876657719
1000 genomesrs876657719
hgdprs876657719
ensemblrs876657719
gopubmedrs876657719
geneviewrs876657719
scholarrs876657719
googlers876657719
pharmgkbrs876657719
gwascentralrs876657719
openSNPrs876657719
23andMers876657719
23andMe allrs876657719
SNP Nexus

SNPshotrs876657719
SNPdbers876657719
MSV3drs876657719
GWAS Ctlgrs876657719
Max Magnitude0
ClinVar
Risk rs876657719(;)
Alt rs876657719(;)
Reference rs876657719(CAAA;CAAA)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene POU3F4
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000023.10:g.82763939_82763942delCAAA
CLNSRC
CLNACC RCV000215388.1,