rs768351915
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs768351915(A;A) |
Make rs768351915(A;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 6 |
Position | 44302059 |
Gene | AARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs768351915 |
dbSNP (classic) | rs768351915 |
ClinGen | rs768351915 |
ebi | rs768351915 |
HLI | rs768351915 |
Exac | rs768351915 |
Gnomad | rs768351915 |
Varsome | rs768351915 |
LitVar | rs768351915 |
Map | rs768351915 |
PheGenI | rs768351915 |
Biobank | rs768351915 |
1000 genomes | rs768351915 |
hgdp | rs768351915 |
ensembl | rs768351915 |
geneview | rs768351915 |
scholar | rs768351915 |
rs768351915 | |
pharmgkb | rs768351915 |
gwascentral | rs768351915 |
openSNP | rs768351915 |
23andMe | rs768351915 |
SNPshot | rs768351915 |
SNPdbe | rs768351915 |
MSV3d | rs768351915 |
GWAS Ctlg | rs768351915 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768351915(A;A) |
Alt | rs768351915(A;A) |
Reference | Rs768351915(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | AARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.44269796C>A |
CLNSRC | |
CLNACC | RCV000384046.1, |