rs387907205
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs387907205(C;C) |
Make rs387907205(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 25227313 |
Gene | KRAS |
is a | snp |
is | mentioned by |
dbSNP | rs387907205 |
dbSNP (classic) | rs387907205 |
ClinGen | rs387907205 |
ebi | rs387907205 |
HLI | rs387907205 |
Exac | rs387907205 |
Gnomad | rs387907205 |
Varsome | rs387907205 |
LitVar | rs387907205 |
Map | rs387907205 |
PheGenI | rs387907205 |
Biobank | rs387907205 |
1000 genomes | rs387907205 |
hgdp | rs387907205 |
ensembl | rs387907205 |
geneview | rs387907205 |
scholar | rs387907205 |
rs387907205 | |
pharmgkb | rs387907205 |
gwascentral | rs387907205 |
openSNP | rs387907205 |
23andMe | rs387907205 |
SNPshot | rs387907205 |
SNPdbe | rs387907205 |
MSV3d | rs387907205 |
GWAS Ctlg | rs387907205 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387907205(C;C) rs387907205(G;G) |
Alt | rs387907205(C;C) rs387907205(G;G) |
Reference | Rs387907205(T;T) |
Significance | Pathogenic |
Disease | Cardiofaciocutaneous syndrome 1 Cardiofaciocutaneous syndrome 2 |
Variation | info |
Gene | KRAS |
CLNDBN | Cardiofaciocutaneous syndrome 1 Cardiofaciocutaneous syndrome 2 |
Reversed | 1 |
HGVS | NC_000012.11:g.25380247A>C; NC_000012.11:g.25380247A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000221667.1, RCV000024617.21, |