rs745595833
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs745595833(C;C) |
Make rs745595833(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32753932 |
Gene | YARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs745595833 |
dbSNP (classic) | rs745595833 |
ClinGen | rs745595833 |
ebi | rs745595833 |
HLI | rs745595833 |
Exac | rs745595833 |
Gnomad | rs745595833 |
Varsome | rs745595833 |
LitVar | rs745595833 |
Map | rs745595833 |
PheGenI | rs745595833 |
Biobank | rs745595833 |
1000 genomes | rs745595833 |
hgdp | rs745595833 |
ensembl | rs745595833 |
geneview | rs745595833 |
scholar | rs745595833 |
rs745595833 | |
pharmgkb | rs745595833 |
gwascentral | rs745595833 |
openSNP | rs745595833 |
23andMe | rs745595833 |
SNPshot | rs745595833 |
SNPdbe | rs745595833 |
MSV3d | rs745595833 |
GWAS Ctlg | rs745595833 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745595833(A;A) rs745595833(C;C) |
Alt | rs745595833(A;A) rs745595833(C;C) |
Reference | Rs745595833(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | YARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.32906866G>C |
CLNSRC | |
CLNACC | RCV000195520.2, |