rs863224057
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs863224057(G;G) |
Make rs863224057(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 43943768 |
Gene | LRPPRC |
is a | snp |
is | mentioned by |
dbSNP | rs863224057 |
dbSNP (classic) | rs863224057 |
ClinGen | rs863224057 |
ebi | rs863224057 |
HLI | rs863224057 |
Exac | rs863224057 |
Gnomad | rs863224057 |
Varsome | rs863224057 |
LitVar | rs863224057 |
Map | rs863224057 |
PheGenI | rs863224057 |
Biobank | rs863224057 |
1000 genomes | rs863224057 |
hgdp | rs863224057 |
ensembl | rs863224057 |
geneview | rs863224057 |
scholar | rs863224057 |
rs863224057 | |
pharmgkb | rs863224057 |
gwascentral | rs863224057 |
openSNP | rs863224057 |
23andMe | rs863224057 |
SNPshot | rs863224057 |
SNPdbe | rs863224057 |
MSV3d | rs863224057 |
GWAS Ctlg | rs863224057 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224057(G;G) |
Alt | rs863224057(G;G) |
Reference | Rs863224057(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LRPPRC |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.44170907A>C |
CLNSRC | |
CLNACC | RCV000198012.2, |