rs773686174
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs773686174(C;T) |
Make rs773686174(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 21 |
Position | 46122147 |
Gene | COL6A2 |
is a | snp |
is | mentioned by |
dbSNP | rs773686174 |
dbSNP (classic) | rs773686174 |
ClinGen | rs773686174 |
ebi | rs773686174 |
HLI | rs773686174 |
Exac | rs773686174 |
Gnomad | rs773686174 |
Varsome | rs773686174 |
LitVar | rs773686174 |
Map | rs773686174 |
PheGenI | rs773686174 |
Biobank | rs773686174 |
1000 genomes | rs773686174 |
hgdp | rs773686174 |
ensembl | rs773686174 |
geneview | rs773686174 |
scholar | rs773686174 |
rs773686174 | |
pharmgkb | rs773686174 |
gwascentral | rs773686174 |
openSNP | rs773686174 |
23andMe | rs773686174 |
SNPshot | rs773686174 |
SNPdbe | rs773686174 |
MSV3d | rs773686174 |
GWAS Ctlg | rs773686174 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773686174(T;T) |
Alt | rs773686174(T;T) |
Reference | Rs773686174(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL6A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.47542061C>T |
CLNSRC | |
CLNACC | RCV000481104.1, |