rs727503109
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs727503109(A;G) |
Make rs727503109(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 25245277 |
Gene | KRAS |
is a | snp |
is | mentioned by |
dbSNP | rs727503109 |
dbSNP (classic) | rs727503109 |
ClinGen | rs727503109 |
ebi | rs727503109 |
HLI | rs727503109 |
Exac | rs727503109 |
Gnomad | rs727503109 |
Varsome | rs727503109 |
LitVar | rs727503109 |
Map | rs727503109 |
PheGenI | rs727503109 |
Biobank | rs727503109 |
1000 genomes | rs727503109 |
hgdp | rs727503109 |
ensembl | rs727503109 |
geneview | rs727503109 |
scholar | rs727503109 |
rs727503109 | |
pharmgkb | rs727503109 |
gwascentral | rs727503109 |
openSNP | rs727503109 |
23andMe | rs727503109 |
SNPshot | rs727503109 |
SNPdbe | rs727503109 |
MSV3d | rs727503109 |
GWAS Ctlg | rs727503109 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727503109(G;G) |
Alt | rs727503109(G;G) |
Reference | Rs727503109(A;A) |
Significance | Probable-Pathogenic |
Disease | Rasopathy not provided |
Variation | info |
Gene | KRAS |
CLNDBN | Rasopathy not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.25398211T>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000150891.1, RCV000260877.1, |