rs4252596
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs4252596(A;A) |
Make rs4252596(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 39699581 |
Gene | ERBB2 |
is a | snp |
is | mentioned by |
dbSNP | rs4252596 |
dbSNP (classic) | rs4252596 |
ClinGen | rs4252596 |
ebi | rs4252596 |
HLI | rs4252596 |
Exac | rs4252596 |
Gnomad | rs4252596 |
Varsome | rs4252596 |
LitVar | rs4252596 |
Map | rs4252596 |
PheGenI | rs4252596 |
Biobank | rs4252596 |
1000 genomes | rs4252596 |
hgdp | rs4252596 |
ensembl | rs4252596 |
geneview | rs4252596 |
scholar | rs4252596 |
rs4252596 | |
pharmgkb | rs4252596 |
gwascentral | rs4252596 |
openSNP | rs4252596 |
23andMe | rs4252596 |
SNPshot | rs4252596 |
SNPdbe | rs4252596 |
MSV3d | rs4252596 |
GWAS Ctlg | rs4252596 |
GMAF | 0.05096 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 17132159] Comprehensive analysis of the ATM, CHEK2 and ERBB2 genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study.
ClinVar | |
---|---|
Risk | rs4252596(A;A) |
Alt | rs4252596(A;A) |
Reference | Rs4252596(C;C) |
Significance | Untested |
Disease | not specified |
Variation | info |
Gene | ERBB2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000017.10:g.37855834C>A |
CLNSRC | ClinVar |
CLNACC | RCV000122379.1, |