rs574088829
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs574088829(A;A) |
Make rs574088829(A;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 39012319 |
Gene | SOS1 |
is a | snp |
is | mentioned by |
dbSNP | rs574088829 |
dbSNP (classic) | rs574088829 |
ClinGen | rs574088829 |
ebi | rs574088829 |
HLI | rs574088829 |
Exac | rs574088829 |
Gnomad | rs574088829 |
Varsome | rs574088829 |
LitVar | rs574088829 |
Map | rs574088829 |
PheGenI | rs574088829 |
Biobank | rs574088829 |
1000 genomes | rs574088829 |
hgdp | rs574088829 |
ensembl | rs574088829 |
geneview | rs574088829 |
scholar | rs574088829 |
rs574088829 | |
pharmgkb | rs574088829 |
gwascentral | rs574088829 |
openSNP | rs574088829 |
23andMe | rs574088829 |
SNPshot | rs574088829 |
SNPdbe | rs574088829 |
MSV3d | rs574088829 |
GWAS Ctlg | rs574088829 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs574088829(A;A) rs574088829(G;G) |
Alt | rs574088829(A;A) rs574088829(G;G) |
Reference | Rs574088829(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SOS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.39239460T>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000159127.1, |