rs200781477
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs200781477(C;C) |
Make rs200781477(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 44301382 |
Gene | AARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs200781477 |
dbSNP (classic) | rs200781477 |
ClinGen | rs200781477 |
ebi | rs200781477 |
HLI | rs200781477 |
Exac | rs200781477 |
Gnomad | rs200781477 |
Varsome | rs200781477 |
LitVar | rs200781477 |
Map | rs200781477 |
PheGenI | rs200781477 |
Biobank | rs200781477 |
1000 genomes | rs200781477 |
hgdp | rs200781477 |
ensembl | rs200781477 |
geneview | rs200781477 |
scholar | rs200781477 |
rs200781477 | |
pharmgkb | rs200781477 |
gwascentral | rs200781477 |
openSNP | rs200781477 |
23andMe | rs200781477 |
SNPshot | rs200781477 |
SNPdbe | rs200781477 |
MSV3d | rs200781477 |
GWAS Ctlg | rs200781477 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200781477(C;C) rs200781477(T;T) |
Alt | rs200781477(C;C) rs200781477(T;T) |
Reference | Rs200781477(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | AARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.44269119G>T |
CLNSRC | |
CLNACC | RCV000200375.1, |