rs541299023
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs541299023(A;A) |
Make rs541299023(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 8013951 |
Gene | GUCY2D |
is a | snp |
is | mentioned by |
dbSNP | rs541299023 |
dbSNP (classic) | rs541299023 |
ClinGen | rs541299023 |
ebi | rs541299023 |
HLI | rs541299023 |
Exac | rs541299023 |
Gnomad | rs541299023 |
Varsome | rs541299023 |
LitVar | rs541299023 |
Map | rs541299023 |
PheGenI | rs541299023 |
Biobank | rs541299023 |
1000 genomes | rs541299023 |
hgdp | rs541299023 |
ensembl | rs541299023 |
geneview | rs541299023 |
scholar | rs541299023 |
rs541299023 | |
pharmgkb | rs541299023 |
gwascentral | rs541299023 |
openSNP | rs541299023 |
23andMe | rs541299023 |
SNPshot | rs541299023 |
SNPdbe | rs541299023 |
MSV3d | rs541299023 |
GWAS Ctlg | rs541299023 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs541299023(A;A) rs541299023(T;T) |
Alt | rs541299023(A;A) rs541299023(T;T) |
Reference | Rs541299023(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GUCY2D |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.7917269G>T |
CLNSRC | |
CLNACC | RCV000478042.1, |