rs376526037
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs376526037(A;A) |
Make rs376526037(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 49483504 |
Gene | ERCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs376526037 |
dbSNP (classic) | rs376526037 |
ClinGen | rs376526037 |
ebi | rs376526037 |
HLI | rs376526037 |
Exac | rs376526037 |
Gnomad | rs376526037 |
Varsome | rs376526037 |
LitVar | rs376526037 |
Map | rs376526037 |
PheGenI | rs376526037 |
Biobank | rs376526037 |
1000 genomes | rs376526037 |
hgdp | rs376526037 |
ensembl | rs376526037 |
geneview | rs376526037 |
scholar | rs376526037 |
rs376526037 | |
pharmgkb | rs376526037 |
gwascentral | rs376526037 |
openSNP | rs376526037 |
23andMe | rs376526037 |
SNPshot | rs376526037 |
SNPdbe | rs376526037 |
MSV3d | rs376526037 |
GWAS Ctlg | rs376526037 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376526037(A;A) |
Alt | rs376526037(A;A) |
Reference | Rs376526037(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ERCC6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.50691550G>A |
CLNSRC | |
CLNACC | RCV000494216.1, |