rs190007694
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs190007694(G;G) |
Make rs190007694(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 43946109 |
Gene | LRPPRC |
is a | snp |
is | mentioned by |
dbSNP | rs190007694 |
dbSNP (classic) | rs190007694 |
ClinGen | rs190007694 |
ebi | rs190007694 |
HLI | rs190007694 |
Exac | rs190007694 |
Gnomad | rs190007694 |
Varsome | rs190007694 |
LitVar | rs190007694 |
Map | rs190007694 |
PheGenI | rs190007694 |
Biobank | rs190007694 |
1000 genomes | rs190007694 |
hgdp | rs190007694 |
ensembl | rs190007694 |
geneview | rs190007694 |
scholar | rs190007694 |
rs190007694 | |
pharmgkb | rs190007694 |
gwascentral | rs190007694 |
openSNP | rs190007694 |
23andMe | rs190007694 |
SNPshot | rs190007694 |
SNPdbe | rs190007694 |
MSV3d | rs190007694 |
GWAS Ctlg | rs190007694 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs190007694(G;G) |
Alt | rs190007694(G;G) |
Reference | Rs190007694(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LRPPRC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.44173248T>G |
CLNSRC | |
CLNACC | RCV000199688.1, |