rs17217772
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs17217772(A;G) |
Make rs17217772(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 47410107 |
Gene | MSH2 |
is a | snp |
is | mentioned by |
dbSNP | rs17217772 |
dbSNP (classic) | rs17217772 |
ClinGen | rs17217772 |
ebi | rs17217772 |
HLI | rs17217772 |
Exac | rs17217772 |
Gnomad | rs17217772 |
Varsome | rs17217772 |
LitVar | rs17217772 |
Map | rs17217772 |
PheGenI | rs17217772 |
Biobank | rs17217772 |
1000 genomes | rs17217772 |
hgdp | rs17217772 |
ensembl | rs17217772 |
geneview | rs17217772 |
scholar | rs17217772 |
rs17217772 | |
pharmgkb | rs17217772 |
gwascentral | rs17217772 |
openSNP | rs17217772 |
23andMe | rs17217772 |
SNPshot | rs17217772 |
SNPdbe | rs17217772 |
MSV3d | rs17217772 |
GWAS Ctlg | rs17217772 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25134804] Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women
ClinVar | |
---|---|
Risk | rs17217772(G;G) rs17217772(T;T) |
Alt | rs17217772(G;G) rs17217772(T;T) |
Reference | Rs17217772(A;A) |
Significance | Non-pathogenic |
Disease | Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MSH2 |
CLNDBN | Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.47637246A>G; NC_000002.11:g.47637246A>T |
CLNSRC | HGMD UniProtKB (protein) |
CLNACC | RCV000030253.4, RCV000035361.8, RCV000144619.1, RCV000162398.1, RCV000076589.2, |