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rs397516336

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs397516336(-;-)
Make rs397516336(-;AT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position83509177
GenePOU3F4
is asnp
is mentioned by
dbSNPrs397516336
ebirs397516336
HLIrs397516336
Exacrs397516336
Varsomers397516336
Maprs397516336
PheGenIrs397516336
hapmaprs397516336
1000 genomesrs397516336
hgdprs397516336
ensemblrs397516336
gopubmedrs397516336
geneviewrs397516336
scholarrs397516336
googlers397516336
pharmgkbrs397516336
gwascentralrs397516336
openSNPrs397516336
23andMers397516336
23andMe allrs397516336
SNP Nexus

SNPshotrs397516336
SNPdbers397516336
MSV3drs397516336
GWAS Ctlgrs397516336
Max Magnitude0
ClinVar
Risk rs397516336(;)
Alt rs397516336(;)
Reference rs397516336(AT;AT)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene POU3F4
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000023.10:g.82764185_82764186delAT
CLNSRC ClinVar
CLNACC RCV000036260.2,