rs201085754
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs201085754(A;C) |
Make rs201085754(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 39056862 |
Gene | SOS1 |
is a | snp |
is | mentioned by |
dbSNP | rs201085754 |
dbSNP (classic) | rs201085754 |
ClinGen | rs201085754 |
ebi | rs201085754 |
HLI | rs201085754 |
Exac | rs201085754 |
Gnomad | rs201085754 |
Varsome | rs201085754 |
LitVar | rs201085754 |
Map | rs201085754 |
PheGenI | rs201085754 |
Biobank | rs201085754 |
1000 genomes | rs201085754 |
hgdp | rs201085754 |
ensembl | rs201085754 |
geneview | rs201085754 |
scholar | rs201085754 |
rs201085754 | |
pharmgkb | rs201085754 |
gwascentral | rs201085754 |
openSNP | rs201085754 |
23andMe | rs201085754 |
SNPshot | rs201085754 |
SNPdbe | rs201085754 |
MSV3d | rs201085754 |
GWAS Ctlg | rs201085754 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201085754(C;C) |
Alt | rs201085754(C;C) |
Reference | Rs201085754(A;A) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | SOS1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.39284003A>C |
CLNSRC | |
CLNACC | RCV000038552.2, |