rs12602083
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs12602083(G;T) |
Make rs12602083(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 17 |
Position | 8016204 |
Gene | GUCY2D |
is a | snp |
is | mentioned by |
dbSNP | rs12602083 |
dbSNP (classic) | rs12602083 |
ClinGen | rs12602083 |
ebi | rs12602083 |
HLI | rs12602083 |
Exac | rs12602083 |
Gnomad | rs12602083 |
Varsome | rs12602083 |
LitVar | rs12602083 |
Map | rs12602083 |
PheGenI | rs12602083 |
Biobank | rs12602083 |
1000 genomes | rs12602083 |
hgdp | rs12602083 |
ensembl | rs12602083 |
geneview | rs12602083 |
scholar | rs12602083 |
rs12602083 | |
pharmgkb | rs12602083 |
gwascentral | rs12602083 |
openSNP | rs12602083 |
23andMe | rs12602083 |
SNPshot | rs12602083 |
SNPdbe | rs12602083 |
MSV3d | rs12602083 |
GWAS Ctlg | rs12602083 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs12602083(C;C) rs12602083(T;T) |
Alt | rs12602083(C;C) rs12602083(T;T) |
Reference | Rs12602083(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GUCY2D |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7919522G>C |
CLNSRC | |
CLNACC | RCV000395581.1, |