rs761796175
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs761796175(A;A) |
Make rs761796175(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 237377336 |
Gene | COL6A3 |
is a | snp |
is | mentioned by |
dbSNP | rs761796175 |
dbSNP (classic) | rs761796175 |
ClinGen | rs761796175 |
ebi | rs761796175 |
HLI | rs761796175 |
Exac | rs761796175 |
Gnomad | rs761796175 |
Varsome | rs761796175 |
LitVar | rs761796175 |
Map | rs761796175 |
PheGenI | rs761796175 |
Biobank | rs761796175 |
1000 genomes | rs761796175 |
hgdp | rs761796175 |
ensembl | rs761796175 |
geneview | rs761796175 |
scholar | rs761796175 |
rs761796175 | |
pharmgkb | rs761796175 |
gwascentral | rs761796175 |
openSNP | rs761796175 |
23andMe | rs761796175 |
SNPshot | rs761796175 |
SNPdbe | rs761796175 |
MSV3d | rs761796175 |
GWAS Ctlg | rs761796175 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761796175(A;A) |
Alt | rs761796175(A;A) |
Reference | Rs761796175(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL6A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.238285979G>A |
CLNSRC | |
CLNACC | RCV000482545.1, |