rs606231202
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs606231202(-;TGG) |
Make rs606231202(TGG;TGG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 25245355 |
Gene | KRAS |
is a | snp |
is | mentioned by |
dbSNP | rs606231202 |
dbSNP (classic) | rs606231202 |
ClinGen | rs606231202 |
ebi | rs606231202 |
HLI | rs606231202 |
Exac | rs606231202 |
Gnomad | rs606231202 |
Varsome | rs606231202 |
LitVar | rs606231202 |
Map | rs606231202 |
PheGenI | rs606231202 |
Biobank | rs606231202 |
1000 genomes | rs606231202 |
hgdp | rs606231202 |
ensembl | rs606231202 |
geneview | rs606231202 |
scholar | rs606231202 |
rs606231202 | |
pharmgkb | rs606231202 |
gwascentral | rs606231202 |
openSNP | rs606231202 |
23andMe | rs606231202 |
SNPshot | rs606231202 |
SNPdbe | rs606231202 |
MSV3d | rs606231202 |
GWAS Ctlg | rs606231202 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs606231202(TGG;TGG) |
Alt | rs606231202(TGG;TGG) |
Reference | Rs606231202(-;-) |
Significance | Pathogenic |
Disease | Acute myeloid leukemia |
Variation | info |
Gene | KRAS |
CLNDBN | Acute myeloid leukemia |
Reversed | 1 |
HGVS | NC_000012.11:g.25398290_25398292dupCCA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000013415.24, |