rs142012387
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs142012387(G;T) |
Make rs142012387(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 70600460 |
Gene | PRF1 |
is a | snp |
is | mentioned by |
dbSNP | rs142012387 |
dbSNP (classic) | rs142012387 |
ClinGen | rs142012387 |
ebi | rs142012387 |
HLI | rs142012387 |
Exac | rs142012387 |
Gnomad | rs142012387 |
Varsome | rs142012387 |
LitVar | rs142012387 |
Map | rs142012387 |
PheGenI | rs142012387 |
Biobank | rs142012387 |
1000 genomes | rs142012387 |
hgdp | rs142012387 |
ensembl | rs142012387 |
geneview | rs142012387 |
scholar | rs142012387 |
rs142012387 | |
pharmgkb | rs142012387 |
gwascentral | rs142012387 |
openSNP | rs142012387 |
23andMe | rs142012387 |
SNPshot | rs142012387 |
SNPdbe | rs142012387 |
MSV3d | rs142012387 |
GWAS Ctlg | rs142012387 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142012387(C;C) rs142012387(T;T) |
Alt | rs142012387(C;C) rs142012387(T;T) |
Reference | Rs142012387(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PRF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.72360216G>C |
CLNSRC | |
CLNACC | RCV000424261.1, |