rs63749985
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs63749985(A;G) |
Make rs63749985(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 87569512 |
Gene | RARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs63749985 |
dbSNP (classic) | rs63749985 |
ClinGen | rs63749985 |
ebi | rs63749985 |
HLI | rs63749985 |
Exac | rs63749985 |
Gnomad | rs63749985 |
Varsome | rs63749985 |
LitVar | rs63749985 |
Map | rs63749985 |
PheGenI | rs63749985 |
Biobank | rs63749985 |
1000 genomes | rs63749985 |
hgdp | rs63749985 |
ensembl | rs63749985 |
geneview | rs63749985 |
scholar | rs63749985 |
rs63749985 | |
pharmgkb | rs63749985 |
gwascentral | rs63749985 |
openSNP | rs63749985 |
23andMe | rs63749985 |
SNPshot | rs63749985 |
SNPdbe | rs63749985 |
MSV3d | rs63749985 |
GWAS Ctlg | rs63749985 |
Max Magnitude | 0 |
[PMID 17847012] Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia.