rs747810875
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs747810875(C;T) |
Make rs747810875(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 107893265 |
Gene | DLD |
is a | snp |
is | mentioned by |
dbSNP | rs747810875 |
dbSNP (classic) | rs747810875 |
ClinGen | rs747810875 |
ebi | rs747810875 |
HLI | rs747810875 |
Exac | rs747810875 |
Gnomad | rs747810875 |
Varsome | rs747810875 |
LitVar | rs747810875 |
Map | rs747810875 |
PheGenI | rs747810875 |
Biobank | rs747810875 |
1000 genomes | rs747810875 |
hgdp | rs747810875 |
ensembl | rs747810875 |
geneview | rs747810875 |
scholar | rs747810875 |
rs747810875 | |
pharmgkb | rs747810875 |
gwascentral | rs747810875 |
openSNP | rs747810875 |
23andMe | rs747810875 |
SNPshot | rs747810875 |
SNPdbe | rs747810875 |
MSV3d | rs747810875 |
GWAS Ctlg | rs747810875 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747810875(G;G) rs747810875(T;T) |
Alt | rs747810875(G;G) rs747810875(T;T) |
Reference | Rs747810875(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | DLD |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000007.13:g.107533710C>G; NC_000007.13:g.107533710C>T |
CLNSRC | |
CLNACC | RCV000479643.1, RCV000252044.1, |