rs530348521
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs530348521(A;A) |
Make rs530348521(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 22 |
Position | 38112559 |
Gene | BAIAP2L2, PLA2G6 |
is a | snp |
is | mentioned by |
dbSNP | rs530348521 |
dbSNP (classic) | rs530348521 |
ClinGen | rs530348521 |
ebi | rs530348521 |
HLI | rs530348521 |
Exac | rs530348521 |
Gnomad | rs530348521 |
Varsome | rs530348521 |
LitVar | rs530348521 |
Map | rs530348521 |
PheGenI | rs530348521 |
Biobank | rs530348521 |
1000 genomes | rs530348521 |
hgdp | rs530348521 |
ensembl | rs530348521 |
geneview | rs530348521 |
scholar | rs530348521 |
rs530348521 | |
pharmgkb | rs530348521 |
gwascentral | rs530348521 |
openSNP | rs530348521 |
23andMe | rs530348521 |
SNPshot | rs530348521 |
SNPdbe | rs530348521 |
MSV3d | rs530348521 |
GWAS Ctlg | rs530348521 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs530348521(A;A) |
Alt | rs530348521(A;A) |
Reference | Rs530348521(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | BAIAP2L2 PLA2G6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.38508566G>A |
CLNSRC | |
CLNACC | RCV000255821.1, |