rs139194636
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs139194636(C;C) |
Make rs139194636(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 119033203 |
Gene | WARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs139194636 |
dbSNP (classic) | rs139194636 |
ClinGen | rs139194636 |
ebi | rs139194636 |
HLI | rs139194636 |
Exac | rs139194636 |
Gnomad | rs139194636 |
Varsome | rs139194636 |
LitVar | rs139194636 |
Map | rs139194636 |
PheGenI | rs139194636 |
Biobank | rs139194636 |
1000 genomes | rs139194636 |
hgdp | rs139194636 |
ensembl | rs139194636 |
geneview | rs139194636 |
scholar | rs139194636 |
rs139194636 | |
pharmgkb | rs139194636 |
gwascentral | rs139194636 |
openSNP | rs139194636 |
23andMe | rs139194636 |
SNPshot | rs139194636 |
SNPdbe | rs139194636 |
MSV3d | rs139194636 |
GWAS Ctlg | rs139194636 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139194636(C;C) |
Alt | rs139194636(C;C) |
Reference | Rs139194636(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | WARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.119575826T>C |
CLNSRC | |
CLNACC | RCV000209945.1, |