rs768344665
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs768344665(-;-) |
Make rs768344665(-;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 32754023 |
Gene | YARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs768344665 |
dbSNP (classic) | rs768344665 |
ClinGen | rs768344665 |
ebi | rs768344665 |
HLI | rs768344665 |
Exac | rs768344665 |
Gnomad | rs768344665 |
Varsome | rs768344665 |
LitVar | rs768344665 |
Map | rs768344665 |
PheGenI | rs768344665 |
Biobank | rs768344665 |
1000 genomes | rs768344665 |
hgdp | rs768344665 |
ensembl | rs768344665 |
geneview | rs768344665 |
scholar | rs768344665 |
rs768344665 | |
pharmgkb | rs768344665 |
gwascentral | rs768344665 |
openSNP | rs768344665 |
23andMe | rs768344665 |
SNPshot | rs768344665 |
SNPdbe | rs768344665 |
MSV3d | rs768344665 |
GWAS Ctlg | rs768344665 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768344665(-;-) |
Alt | rs768344665(-;-) |
Reference | Rs768344665(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | YARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.32906957delT |
CLNSRC | |
CLNACC | RCV000479623.1, |