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rs727505246

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505246(A;A)
Make rs727505246(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position83509292
GenePOU3F4
is asnp
is mentioned by
dbSNPrs727505246
ebirs727505246
HLIrs727505246
Exacrs727505246
Varsomers727505246
Maprs727505246
PheGenIrs727505246
hapmaprs727505246
1000 genomesrs727505246
hgdprs727505246
ensemblrs727505246
gopubmedrs727505246
geneviewrs727505246
scholarrs727505246
googlers727505246
pharmgkbrs727505246
gwascentralrs727505246
openSNPrs727505246
23andMers727505246
23andMe allrs727505246
SNP Nexus

SNPshotrs727505246
SNPdbers727505246
MSV3drs727505246
GWAS Ctlgrs727505246
Max Magnitude0
ClinVar
Risk rs727505246(A;A)
Alt rs727505246(A;A)
Reference rs727505246(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene POU3F4
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000023.10:g.82764300G>A
CLNSRC
CLNACC RCV000156766.2,