rs121913527
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121913527(A;A) |
Make rs121913527(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 25225628 |
Gene | KRAS |
is a | snp |
is | mentioned by |
dbSNP | rs121913527 |
dbSNP (classic) | rs121913527 |
ClinGen | rs121913527 |
ebi | rs121913527 |
HLI | rs121913527 |
Exac | rs121913527 |
Gnomad | rs121913527 |
Varsome | rs121913527 |
LitVar | rs121913527 |
Map | rs121913527 |
PheGenI | rs121913527 |
Biobank | rs121913527 |
1000 genomes | rs121913527 |
hgdp | rs121913527 |
ensembl | rs121913527 |
geneview | rs121913527 |
scholar | rs121913527 |
rs121913527 | |
pharmgkb | rs121913527 |
gwascentral | rs121913527 |
openSNP | rs121913527 |
23andMe | rs121913527 |
SNPshot | rs121913527 |
SNPdbe | rs121913527 |
MSV3d | rs121913527 |
GWAS Ctlg | rs121913527 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913527(A;A) rs121913527(C;C) rs121913527(T;T) |
Alt | rs121913527(A;A) rs121913527(C;C) rs121913527(T;T) |
Reference | Rs121913527(G;G) |
Significance | Pathogenic |
Disease | Rasopathy Colorectal Neoplasms not specified |
Variation | info |
Gene | KRAS |
CLNDBN | Rasopathy Colorectal Neoplasms not specified |
Reversed | 1 |
HGVS | NC_000012.11:g.25378562C>A; NC_000012.11:g.25378562C>G; NC_000012.11:g.25378562C>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000473918.1, RCV000444020.1, RCV000178223.1, RCV000426420.1, |