rs760446904
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs760446904(C;T) |
Make rs760446904(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 237361132 |
Gene | COL6A3 |
is a | snp |
is | mentioned by |
dbSNP | rs760446904 |
dbSNP (classic) | rs760446904 |
ClinGen | rs760446904 |
ebi | rs760446904 |
HLI | rs760446904 |
Exac | rs760446904 |
Gnomad | rs760446904 |
Varsome | rs760446904 |
LitVar | rs760446904 |
Map | rs760446904 |
PheGenI | rs760446904 |
Biobank | rs760446904 |
1000 genomes | rs760446904 |
hgdp | rs760446904 |
ensembl | rs760446904 |
geneview | rs760446904 |
scholar | rs760446904 |
rs760446904 | |
pharmgkb | rs760446904 |
gwascentral | rs760446904 |
openSNP | rs760446904 |
23andMe | rs760446904 |
SNPshot | rs760446904 |
SNPdbe | rs760446904 |
MSV3d | rs760446904 |
GWAS Ctlg | rs760446904 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs760446904(T;T) |
Alt | rs760446904(T;T) |
Reference | Rs760446904(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | COL6A3 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.238269775C>T |
CLNSRC | |
CLNACC | RCV000274706.1, RCV000494333.1, |