rs1085307627
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Chromosome | 3 |
Position | 42688263 |
Gene | KLHL40 |
is a | snp |
is | mentioned by |
dbSNP | rs1085307627 |
dbSNP (classic) | rs1085307627 |
ClinGen | rs1085307627 |
ebi | rs1085307627 |
HLI | rs1085307627 |
Exac | rs1085307627 |
Gnomad | rs1085307627 |
Varsome | rs1085307627 |
LitVar | rs1085307627 |
Map | rs1085307627 |
PheGenI | rs1085307627 |
Biobank | rs1085307627 |
1000 genomes | rs1085307627 |
hgdp | rs1085307627 |
ensembl | rs1085307627 |
geneview | rs1085307627 |
scholar | rs1085307627 |
rs1085307627 | |
pharmgkb | rs1085307627 |
gwascentral | rs1085307627 |
openSNP | rs1085307627 |
23andMe | rs1085307627 |
SNPshot | rs1085307627 |
SNPdbe | rs1085307627 |
MSV3d | rs1085307627 |
GWAS Ctlg | rs1085307627 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1085307627(G;G) |
Alt | rs1085307627(G;G) |
Reference | Rs1085307627(-;-) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | KLHL40 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.42729755dup |
CLNSRC | |
CLNACC | RCV000489024.1, |