rs113605136
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs113605136(C;G) |
Make rs113605136(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 237359089 |
Gene | COL6A3 |
is a | snp |
is | mentioned by |
dbSNP | rs113605136 |
dbSNP (classic) | rs113605136 |
ClinGen | rs113605136 |
ebi | rs113605136 |
HLI | rs113605136 |
Exac | rs113605136 |
Gnomad | rs113605136 |
Varsome | rs113605136 |
LitVar | rs113605136 |
Map | rs113605136 |
PheGenI | rs113605136 |
Biobank | rs113605136 |
1000 genomes | rs113605136 |
hgdp | rs113605136 |
ensembl | rs113605136 |
geneview | rs113605136 |
scholar | rs113605136 |
rs113605136 | |
pharmgkb | rs113605136 |
gwascentral | rs113605136 |
openSNP | rs113605136 |
23andMe | rs113605136 |
SNPshot | rs113605136 |
SNPdbe | rs113605136 |
MSV3d | rs113605136 |
GWAS Ctlg | rs113605136 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs113605136(A;A) rs113605136(G;G) rs113605136(T;T) |
Alt | rs113605136(A;A) rs113605136(G;G) rs113605136(T;T) |
Reference | Rs113605136(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL6A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.238267732C>T |
CLNSRC | |
CLNACC | RCV000397729.1, |