rs1085307647
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 17 |
Position | 44868286 |
Gene | EFTUD2 |
is a | snp |
is | mentioned by |
dbSNP | rs1085307647 |
dbSNP (classic) | rs1085307647 |
ClinGen | rs1085307647 |
ebi | rs1085307647 |
HLI | rs1085307647 |
Exac | rs1085307647 |
Gnomad | rs1085307647 |
Varsome | rs1085307647 |
LitVar | rs1085307647 |
Map | rs1085307647 |
PheGenI | rs1085307647 |
Biobank | rs1085307647 |
1000 genomes | rs1085307647 |
hgdp | rs1085307647 |
ensembl | rs1085307647 |
geneview | rs1085307647 |
scholar | rs1085307647 |
rs1085307647 | |
pharmgkb | rs1085307647 |
gwascentral | rs1085307647 |
openSNP | rs1085307647 |
23andMe | rs1085307647 |
SNPshot | rs1085307647 |
SNPdbe | rs1085307647 |
MSV3d | rs1085307647 |
GWAS Ctlg | rs1085307647 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1085307647(A;A) |
Alt | rs1085307647(A;A) |
Reference | Rs1085307647(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | EFTUD2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.42945654C>T |
CLNSRC | |
CLNACC | RCV000488992.1, |