rs555093151
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs555093151(C;C) |
Make rs555093151(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 32755694 |
Gene | YARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs555093151 |
dbSNP (classic) | rs555093151 |
ClinGen | rs555093151 |
ebi | rs555093151 |
HLI | rs555093151 |
Exac | rs555093151 |
Gnomad | rs555093151 |
Varsome | rs555093151 |
LitVar | rs555093151 |
Map | rs555093151 |
PheGenI | rs555093151 |
Biobank | rs555093151 |
1000 genomes | rs555093151 |
hgdp | rs555093151 |
ensembl | rs555093151 |
geneview | rs555093151 |
scholar | rs555093151 |
rs555093151 | |
pharmgkb | rs555093151 |
gwascentral | rs555093151 |
openSNP | rs555093151 |
23andMe | rs555093151 |
SNPshot | rs555093151 |
SNPdbe | rs555093151 |
MSV3d | rs555093151 |
GWAS Ctlg | rs555093151 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs555093151(A;A) rs555093151(C;C) |
Alt | rs555093151(A;A) rs555093151(C;C) |
Reference | Rs555093151(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | YARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.32908628G>C |
CLNSRC | |
CLNACC | RCV000433553.1, |