rs757649757
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs757649757(A;G) |
Make rs757649757(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 197705550 |
Gene | MARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs757649757 |
dbSNP (classic) | rs757649757 |
ClinGen | rs757649757 |
ebi | rs757649757 |
HLI | rs757649757 |
Exac | rs757649757 |
Gnomad | rs757649757 |
Varsome | rs757649757 |
LitVar | rs757649757 |
Map | rs757649757 |
PheGenI | rs757649757 |
Biobank | rs757649757 |
1000 genomes | rs757649757 |
hgdp | rs757649757 |
ensembl | rs757649757 |
geneview | rs757649757 |
scholar | rs757649757 |
rs757649757 | |
pharmgkb | rs757649757 |
gwascentral | rs757649757 |
openSNP | rs757649757 |
23andMe | rs757649757 |
SNPshot | rs757649757 |
SNPdbe | rs757649757 |
MSV3d | rs757649757 |
GWAS Ctlg | rs757649757 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757649757(G;G) |
Alt | rs757649757(G;G) |
Reference | Rs757649757(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.198570274A>G |
CLNSRC | |
CLNACC | RCV000195832.1, |