rs876661059
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs876661059(-;-) |
Make rs876661059(-;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 37020454 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs876661059 |
dbSNP (classic) | rs876661059 |
ClinGen | rs876661059 |
ebi | rs876661059 |
HLI | rs876661059 |
Exac | rs876661059 |
Gnomad | rs876661059 |
Varsome | rs876661059 |
LitVar | rs876661059 |
Map | rs876661059 |
PheGenI | rs876661059 |
Biobank | rs876661059 |
1000 genomes | rs876661059 |
hgdp | rs876661059 |
ensembl | rs876661059 |
geneview | rs876661059 |
scholar | rs876661059 |
rs876661059 | |
pharmgkb | rs876661059 |
gwascentral | rs876661059 |
openSNP | rs876661059 |
23andMe | rs876661059 |
SNPshot | rs876661059 |
SNPdbe | rs876661059 |
MSV3d | rs876661059 |
GWAS Ctlg | rs876661059 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661059(-;-) |
Alt | rs876661059(-;-) |
Reference | Rs876661059(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MLH1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.37061945delC |
CLNSRC | |
CLNACC | RCV000219234.1, |