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

rs866754647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs866754647(A;A)
Make rs866754647(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position83508971
GenePOU3F4
is asnp
is mentioned by
dbSNPrs866754647
dbSNP (classic)rs866754647
ClinGenrs866754647
ebirs866754647
HLIrs866754647
Exacrs866754647
Gnomadrs866754647
Varsomers866754647
LitVarrs866754647
Maprs866754647
PheGenIrs866754647
Biobankrs866754647
1000 genomesrs866754647
hgdprs866754647
ensemblrs866754647
geneviewrs866754647
scholarrs866754647
googlers866754647
pharmgkbrs866754647
gwascentralrs866754647
openSNPrs866754647
23andMers866754647
SNPshotrs866754647
SNPdbers866754647
MSV3drs866754647
GWAS Ctlgrs866754647
Max Magnitude0
ClinVar
Risk rs866754647(A;A)
Alt rs866754647(A;A)
Reference Rs866754647(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POU3F4
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.82763979G>A
CLNSRC
CLNACC RCV000480190.1,