rs368497893
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs368497893(C;T) |
Make rs368497893(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 22 |
Position | 38132831 |
Gene | PLA2G6 |
is a | snp |
is | mentioned by |
dbSNP | rs368497893 |
dbSNP (classic) | rs368497893 |
ClinGen | rs368497893 |
ebi | rs368497893 |
HLI | rs368497893 |
Exac | rs368497893 |
Gnomad | rs368497893 |
Varsome | rs368497893 |
LitVar | rs368497893 |
Map | rs368497893 |
PheGenI | rs368497893 |
Biobank | rs368497893 |
1000 genomes | rs368497893 |
hgdp | rs368497893 |
ensembl | rs368497893 |
geneview | rs368497893 |
scholar | rs368497893 |
rs368497893 | |
pharmgkb | rs368497893 |
gwascentral | rs368497893 |
openSNP | rs368497893 |
23andMe | rs368497893 |
SNPshot | rs368497893 |
SNPdbe | rs368497893 |
MSV3d | rs368497893 |
GWAS Ctlg | rs368497893 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs368497893(T;T) |
Alt | rs368497893(T;T) |
Reference | Rs368497893(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PLA2G6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.38528838C>T |
CLNSRC | |
CLNACC | RCV000266508.1, |