rs2070863
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2070863(C;T) |
Make rs2070863(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 1745208 |
Gene | SERPINF2 |
is a | snp |
is | mentioned by |
dbSNP | rs2070863 |
dbSNP (classic) | rs2070863 |
ClinGen | rs2070863 |
ebi | rs2070863 |
HLI | rs2070863 |
Exac | rs2070863 |
Gnomad | rs2070863 |
Varsome | rs2070863 |
LitVar | rs2070863 |
Map | rs2070863 |
PheGenI | rs2070863 |
Biobank | rs2070863 |
1000 genomes | rs2070863 |
hgdp | rs2070863 |
ensembl | rs2070863 |
geneview | rs2070863 |
scholar | rs2070863 |
rs2070863 | |
pharmgkb | rs2070863 |
gwascentral | rs2070863 |
openSNP | rs2070863 |
23andMe | rs2070863 |
SNPshot | rs2070863 |
SNPdbe | rs2070863 |
MSV3d | rs2070863 |
GWAS Ctlg | rs2070863 |
GMAF | 0.1915 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs2070863(T;T) |
Alt | rs2070863(T;T) |
Reference | Rs2070863(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | SERPINF2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000017.10:g.1648502C>T |
CLNSRC | |
CLNACC | RCV000242389.1, |