rs757156390
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs757156390(A;A) |
Make rs757156390(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 123332657 |
Gene | ADCY5 |
is a | snp |
is | mentioned by |
dbSNP | rs757156390 |
dbSNP (classic) | rs757156390 |
ClinGen | rs757156390 |
ebi | rs757156390 |
HLI | rs757156390 |
Exac | rs757156390 |
Gnomad | rs757156390 |
Varsome | rs757156390 |
LitVar | rs757156390 |
Map | rs757156390 |
PheGenI | rs757156390 |
Biobank | rs757156390 |
1000 genomes | rs757156390 |
hgdp | rs757156390 |
ensembl | rs757156390 |
geneview | rs757156390 |
scholar | rs757156390 |
rs757156390 | |
pharmgkb | rs757156390 |
gwascentral | rs757156390 |
openSNP | rs757156390 |
23andMe | rs757156390 |
SNPshot | rs757156390 |
SNPdbe | rs757156390 |
MSV3d | rs757156390 |
GWAS Ctlg | rs757156390 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757156390(A;A) rs757156390(C;C) |
Alt | rs757156390(A;A) rs757156390(C;C) |
Reference | Rs757156390(G;G) |
Significance | Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | ADCY5 |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000003.11:g.123051504G>C |
CLNSRC | |
CLNACC | RCV000190681.1, |