rs757094189
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs757094189(C;C) |
Make rs757094189(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 39013522 |
Gene | SOS1 |
is a | snp |
is | mentioned by |
dbSNP | rs757094189 |
dbSNP (classic) | rs757094189 |
ClinGen | rs757094189 |
ebi | rs757094189 |
HLI | rs757094189 |
Exac | rs757094189 |
Gnomad | rs757094189 |
Varsome | rs757094189 |
LitVar | rs757094189 |
Map | rs757094189 |
PheGenI | rs757094189 |
Biobank | rs757094189 |
1000 genomes | rs757094189 |
hgdp | rs757094189 |
ensembl | rs757094189 |
geneview | rs757094189 |
scholar | rs757094189 |
rs757094189 | |
pharmgkb | rs757094189 |
gwascentral | rs757094189 |
openSNP | rs757094189 |
23andMe | rs757094189 |
SNPshot | rs757094189 |
SNPdbe | rs757094189 |
MSV3d | rs757094189 |
GWAS Ctlg | rs757094189 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757094189(C;C) |
Alt | rs757094189(C;C) |
Reference | Rs757094189(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SOS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.39240663T>C |
CLNSRC | |
CLNACC | RCV000171288.1, |