rs184830847
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs184830847(A;A) |
Make rs184830847(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 95103721 |
Gene | DICER1 |
is a | snp |
is | mentioned by |
dbSNP | rs184830847 |
dbSNP (classic) | rs184830847 |
ClinGen | rs184830847 |
ebi | rs184830847 |
HLI | rs184830847 |
Exac | rs184830847 |
Gnomad | rs184830847 |
Varsome | rs184830847 |
LitVar | rs184830847 |
Map | rs184830847 |
PheGenI | rs184830847 |
Biobank | rs184830847 |
1000 genomes | rs184830847 |
hgdp | rs184830847 |
ensembl | rs184830847 |
geneview | rs184830847 |
scholar | rs184830847 |
rs184830847 | |
pharmgkb | rs184830847 |
gwascentral | rs184830847 |
openSNP | rs184830847 |
23andMe | rs184830847 |
SNPshot | rs184830847 |
SNPdbe | rs184830847 |
MSV3d | rs184830847 |
GWAS Ctlg | rs184830847 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs184830847(A;A) |
Alt | rs184830847(A;A) |
Reference | Rs184830847(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | DICER1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000014.8:g.95570058G>C |
CLNSRC | |
CLNACC | RCV000494286.1, |