rs1036185928
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1036185928(C;T) |
Make rs1036185928(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 40349931 |
Gene | ADSL |
is a | snp |
is | mentioned by |
dbSNP | rs1036185928 |
dbSNP (classic) | rs1036185928 |
ClinGen | rs1036185928 |
ebi | rs1036185928 |
HLI | rs1036185928 |
Exac | rs1036185928 |
Gnomad | rs1036185928 |
Varsome | rs1036185928 |
LitVar | rs1036185928 |
Map | rs1036185928 |
PheGenI | rs1036185928 |
Biobank | rs1036185928 |
1000 genomes | rs1036185928 |
hgdp | rs1036185928 |
ensembl | rs1036185928 |
geneview | rs1036185928 |
scholar | rs1036185928 |
rs1036185928 | |
pharmgkb | rs1036185928 |
gwascentral | rs1036185928 |
openSNP | rs1036185928 |
23andMe | rs1036185928 |
SNPshot | rs1036185928 |
SNPdbe | rs1036185928 |
MSV3d | rs1036185928 |
GWAS Ctlg | rs1036185928 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1036185928(T;T) |
Alt | rs1036185928(T;T) |
Reference | Rs1036185928(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADSL |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.40745935C>T |
CLNSRC | |
CLNACC | RCV000434653.1, |