rs763303046
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs763303046(A;T) |
Make rs763303046(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 107901780 |
Gene | DLD |
is a | snp |
is | mentioned by |
dbSNP | rs763303046 |
dbSNP (classic) | rs763303046 |
ClinGen | rs763303046 |
ebi | rs763303046 |
HLI | rs763303046 |
Exac | rs763303046 |
Gnomad | rs763303046 |
Varsome | rs763303046 |
LitVar | rs763303046 |
Map | rs763303046 |
PheGenI | rs763303046 |
Biobank | rs763303046 |
1000 genomes | rs763303046 |
hgdp | rs763303046 |
ensembl | rs763303046 |
geneview | rs763303046 |
scholar | rs763303046 |
rs763303046 | |
pharmgkb | rs763303046 |
gwascentral | rs763303046 |
openSNP | rs763303046 |
23andMe | rs763303046 |
SNPshot | rs763303046 |
SNPdbe | rs763303046 |
MSV3d | rs763303046 |
GWAS Ctlg | rs763303046 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763303046(G;G) rs763303046(T;T) |
Alt | rs763303046(G;G) rs763303046(T;T) |
Reference | Rs763303046(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DLD |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.107542225A>G |
CLNSRC | |
CLNACC | RCV000484591.1, |