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

rs759091617

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759091617(A;A)
Make rs759091617(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position146340275
GenePOU4F3
is asnp
is mentioned by
dbSNPrs759091617
ebirs759091617
HLIrs759091617
Exacrs759091617
Varsomers759091617
Maprs759091617
PheGenIrs759091617
hapmaprs759091617
1000 genomesrs759091617
hgdprs759091617
ensemblrs759091617
gopubmedrs759091617
geneviewrs759091617
scholarrs759091617
googlers759091617
pharmgkbrs759091617
gwascentralrs759091617
openSNPrs759091617
23andMers759091617
23andMe allrs759091617
SNP Nexus

SNPshotrs759091617
SNPdbers759091617
MSV3drs759091617
GWAS Ctlgrs759091617
Max Magnitude0
ClinVar
Risk rs759091617(A;A)
Alt rs759091617(A;A)
Reference rs759091617(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POU4F3
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.145719838C>T
CLNSRC
CLNACC RCV000171386.1,