rs1801201
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs1801201(A;G) |
Make rs1801201(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 39723332 |
Gene | ERBB2 |
is a | snp |
is | mentioned by |
dbSNP | rs1801201 |
dbSNP (classic) | rs1801201 |
ClinGen | rs1801201 |
ebi | rs1801201 |
HLI | rs1801201 |
Exac | rs1801201 |
Gnomad | rs1801201 |
Varsome | rs1801201 |
LitVar | rs1801201 |
Map | rs1801201 |
PheGenI | rs1801201 |
Biobank | rs1801201 |
1000 genomes | rs1801201 |
hgdp | rs1801201 |
ensembl | rs1801201 |
geneview | rs1801201 |
scholar | rs1801201 |
rs1801201 | |
pharmgkb | rs1801201 |
gwascentral | rs1801201 |
openSNP | rs1801201 |
23andMe | rs1801201 |
SNPshot | rs1801201 |
SNPdbe | rs1801201 |
MSV3d | rs1801201 |
GWAS Ctlg | rs1801201 |
GMAF | 0.002755 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1801201(C;C) rs1801201(G;G) |
Alt | rs1801201(C;C) rs1801201(G;G) |
Reference | Rs1801201(A;A) |
Significance | Non-pathogenic |
Disease | ERBB2 POLYMORPHISM not specified |
Variation | info |
Gene | ERBB2 |
CLNDBN | ERBB2 POLYMORPHISM not specified |
Reversed | 0 |
HGVS | NC_000017.10:g.37879585A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014888.2, RCV000120743.1, |
[PMID 19124506] Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.
[PMID 19336545] Heritable variation of ERBB2 and breast cancer risk.