rs757169781
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs757169781(A;T) |
Make rs757169781(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 44313103 |
Gene | AARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs757169781 |
dbSNP (classic) | rs757169781 |
ClinGen | rs757169781 |
ebi | rs757169781 |
HLI | rs757169781 |
Exac | rs757169781 |
Gnomad | rs757169781 |
Varsome | rs757169781 |
LitVar | rs757169781 |
Map | rs757169781 |
PheGenI | rs757169781 |
Biobank | rs757169781 |
1000 genomes | rs757169781 |
hgdp | rs757169781 |
ensembl | rs757169781 |
geneview | rs757169781 |
scholar | rs757169781 |
rs757169781 | |
pharmgkb | rs757169781 |
gwascentral | rs757169781 |
openSNP | rs757169781 |
23andMe | rs757169781 |
SNPshot | rs757169781 |
SNPdbe | rs757169781 |
MSV3d | rs757169781 |
GWAS Ctlg | rs757169781 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757169781(T;T) |
Alt | rs757169781(T;T) |
Reference | Rs757169781(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | AARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.44280840A>T |
CLNSRC | |
CLNACC | RCV000195876.1, |