rs745990956
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs745990956(A;A) |
Make rs745990956(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 20 |
Position | 25300853 |
Gene | ABHD12 |
is a | snp |
is | mentioned by |
dbSNP | rs745990956 |
dbSNP (classic) | rs745990956 |
ClinGen | rs745990956 |
ebi | rs745990956 |
HLI | rs745990956 |
Exac | rs745990956 |
Gnomad | rs745990956 |
Varsome | rs745990956 |
LitVar | rs745990956 |
Map | rs745990956 |
PheGenI | rs745990956 |
Biobank | rs745990956 |
1000 genomes | rs745990956 |
hgdp | rs745990956 |
ensembl | rs745990956 |
geneview | rs745990956 |
scholar | rs745990956 |
rs745990956 | |
pharmgkb | rs745990956 |
gwascentral | rs745990956 |
openSNP | rs745990956 |
23andMe | rs745990956 |
SNPshot | rs745990956 |
SNPdbe | rs745990956 |
MSV3d | rs745990956 |
GWAS Ctlg | rs745990956 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745990956(A;A) |
Alt | rs745990956(A;A) |
Reference | Rs745990956(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABHD12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.25281489G>A |
CLNSRC | |
CLNACC | RCV000171343.1, |