rs730881003
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs730881003(C;C) |
Make rs730881003(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 12585794 |
Gene | RAF1 |
is a | snp |
is | mentioned by |
dbSNP | rs730881003 |
dbSNP (classic) | rs730881003 |
ClinGen | rs730881003 |
ebi | rs730881003 |
HLI | rs730881003 |
Exac | rs730881003 |
Gnomad | rs730881003 |
Varsome | rs730881003 |
LitVar | rs730881003 |
Map | rs730881003 |
PheGenI | rs730881003 |
Biobank | rs730881003 |
1000 genomes | rs730881003 |
hgdp | rs730881003 |
ensembl | rs730881003 |
geneview | rs730881003 |
scholar | rs730881003 |
rs730881003 | |
pharmgkb | rs730881003 |
gwascentral | rs730881003 |
openSNP | rs730881003 |
23andMe | rs730881003 |
SNPshot | rs730881003 |
SNPdbe | rs730881003 |
MSV3d | rs730881003 |
GWAS Ctlg | rs730881003 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881003(C;C) |
Alt | rs730881003(C;C) |
Reference | Rs730881003(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | RAF1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.12627293A>G |
CLNSRC | |
CLNACC | RCV000159085.1, |