rs863224182
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs863224182(-;G) |
Make rs863224182(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 87524632 |
Gene | RARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs863224182 |
dbSNP (classic) | rs863224182 |
ClinGen | rs863224182 |
ebi | rs863224182 |
HLI | rs863224182 |
Exac | rs863224182 |
Gnomad | rs863224182 |
Varsome | rs863224182 |
LitVar | rs863224182 |
Map | rs863224182 |
PheGenI | rs863224182 |
Biobank | rs863224182 |
1000 genomes | rs863224182 |
hgdp | rs863224182 |
ensembl | rs863224182 |
geneview | rs863224182 |
scholar | rs863224182 |
rs863224182 | |
pharmgkb | rs863224182 |
gwascentral | rs863224182 |
openSNP | rs863224182 |
23andMe | rs863224182 |
SNPshot | rs863224182 |
SNPdbe | rs863224182 |
MSV3d | rs863224182 |
GWAS Ctlg | rs863224182 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224182(G;G) |
Alt | rs863224182(G;G) |
Reference | Rs863224182(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | RARS2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.88234351dupC |
CLNSRC | |
CLNACC | RCV000199506.1, |