rs764611160
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
Make rs764611160(-;-) |
Make rs764611160(-;AG) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 107915624 |
Gene | DLD |
is a | snp |
is | mentioned by |
dbSNP | rs764611160 |
dbSNP (classic) | rs764611160 |
ClinGen | rs764611160 |
ebi | rs764611160 |
HLI | rs764611160 |
Exac | rs764611160 |
Gnomad | rs764611160 |
Varsome | rs764611160 |
LitVar | rs764611160 |
Map | rs764611160 |
PheGenI | rs764611160 |
Biobank | rs764611160 |
1000 genomes | rs764611160 |
hgdp | rs764611160 |
ensembl | rs764611160 |
geneview | rs764611160 |
scholar | rs764611160 |
rs764611160 | |
pharmgkb | rs764611160 |
gwascentral | rs764611160 |
openSNP | rs764611160 |
23andMe | rs764611160 |
SNPshot | rs764611160 |
SNPdbe | rs764611160 |
MSV3d | rs764611160 |
GWAS Ctlg | rs764611160 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs764611160(-;-) |
Alt | rs764611160(-;-) |
Reference | Rs764611160(AG;AG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DLD |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.107556069_107556070delAG |
CLNSRC | |
CLNACC | RCV000482561.1, |