rs142932960
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs142932960(A;A) |
Make rs142932960(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 9839148 |
Gene | RPUSD3 |
is a | snp |
is | mentioned by |
dbSNP | rs142932960 |
dbSNP (classic) | rs142932960 |
ClinGen | rs142932960 |
ebi | rs142932960 |
HLI | rs142932960 |
Exac | rs142932960 |
Gnomad | rs142932960 |
Varsome | rs142932960 |
LitVar | rs142932960 |
Map | rs142932960 |
PheGenI | rs142932960 |
Biobank | rs142932960 |
1000 genomes | rs142932960 |
hgdp | rs142932960 |
ensembl | rs142932960 |
geneview | rs142932960 |
scholar | rs142932960 |
rs142932960 | |
pharmgkb | rs142932960 |
gwascentral | rs142932960 |
openSNP | rs142932960 |
23andMe | rs142932960 |
SNPshot | rs142932960 |
SNPdbe | rs142932960 |
MSV3d | rs142932960 |
GWAS Ctlg | rs142932960 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142932960(A;A) |
Alt | rs142932960(A;A) |
Reference | Rs142932960(G;G) |
Significance | Probable-Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | RPUSD3 |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000003.11:g.9880832G>A |
CLNSRC | |
CLNACC | RCV000210730.1, |