rs3219466
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs3219466(C;T) |
Make rs3219466(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 45340381 |
Gene | MUTYH, TOE1 |
is a | snp |
is | mentioned by |
dbSNP | rs3219466 |
dbSNP (classic) | rs3219466 |
ClinGen | rs3219466 |
ebi | rs3219466 |
HLI | rs3219466 |
Exac | rs3219466 |
Gnomad | rs3219466 |
Varsome | rs3219466 |
LitVar | rs3219466 |
Map | rs3219466 |
PheGenI | rs3219466 |
Biobank | rs3219466 |
1000 genomes | rs3219466 |
hgdp | rs3219466 |
ensembl | rs3219466 |
geneview | rs3219466 |
scholar | rs3219466 |
rs3219466 | |
pharmgkb | rs3219466 |
gwascentral | rs3219466 |
openSNP | rs3219466 |
23andMe | rs3219466 |
SNPshot | rs3219466 |
SNPdbe | rs3219466 |
MSV3d | rs3219466 |
GWAS Ctlg | rs3219466 |
GMAF | 0.01331 |
Max Magnitude | 0 |
[PMID 20150366] DNA repair gene polymorphisms and risk of adult meningioma, glioma, and acoustic neuroma [PMID 19029194] Base excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African-Americans.
[PMID 22687647] Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population.
ClinVar | |
---|---|
Risk | rs3219466(A;A) rs3219466(T;T) |
Alt | rs3219466(A;A) rs3219466(T;T) |
Reference | Rs3219466(C;C) |
Significance | Unknown |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | TOE1 MUTYH |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000001.10:g.45806053G>A |
CLNSRC | |
CLNACC | RCV000491011.1, |