rs759091617
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs759091617(A;A) |
Make rs759091617(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 146340275 |
Gene | POU4F3 |
is a | snp |
is | mentioned by |
dbSNP | rs759091617 |
dbSNP (classic) | rs759091617 |
ClinGen | rs759091617 |
ebi | rs759091617 |
HLI | rs759091617 |
Exac | rs759091617 |
Gnomad | rs759091617 |
Varsome | rs759091617 |
LitVar | rs759091617 |
Map | rs759091617 |
PheGenI | rs759091617 |
Biobank | rs759091617 |
1000 genomes | rs759091617 |
hgdp | rs759091617 |
ensembl | rs759091617 |
geneview | rs759091617 |
scholar | rs759091617 |
rs759091617 | |
pharmgkb | rs759091617 |
gwascentral | rs759091617 |
openSNP | rs759091617 |
23andMe | rs759091617 |
SNPshot | rs759091617 |
SNPdbe | rs759091617 |
MSV3d | rs759091617 |
GWAS Ctlg | rs759091617 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759091617(A;A) rs759091617(T;T) |
Alt | rs759091617(A;A) rs759091617(T;T) |
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, |