rs148921184
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs148921184(A;A) |
Make rs148921184(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 5771341 |
Gene | FARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs148921184 |
dbSNP (classic) | rs148921184 |
ClinGen | rs148921184 |
ebi | rs148921184 |
HLI | rs148921184 |
Exac | rs148921184 |
Gnomad | rs148921184 |
Varsome | rs148921184 |
LitVar | rs148921184 |
Map | rs148921184 |
PheGenI | rs148921184 |
Biobank | rs148921184 |
1000 genomes | rs148921184 |
hgdp | rs148921184 |
ensembl | rs148921184 |
geneview | rs148921184 |
scholar | rs148921184 |
rs148921184 | |
pharmgkb | rs148921184 |
gwascentral | rs148921184 |
openSNP | rs148921184 |
23andMe | rs148921184 |
SNPshot | rs148921184 |
SNPdbe | rs148921184 |
MSV3d | rs148921184 |
GWAS Ctlg | rs148921184 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148921184(A;A) |
Alt | rs148921184(A;A) |
Reference | Rs148921184(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.5771574G>A |
CLNSRC | |
CLNACC | RCV000198469.1, |