rs1085307743
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 1 |
Position | 7640516 |
Gene | CAMTA1 |
is a | snp |
is | mentioned by |
dbSNP | rs1085307743 |
dbSNP (classic) | rs1085307743 |
ClinGen | rs1085307743 |
ebi | rs1085307743 |
HLI | rs1085307743 |
Exac | rs1085307743 |
Gnomad | rs1085307743 |
Varsome | rs1085307743 |
LitVar | rs1085307743 |
Map | rs1085307743 |
PheGenI | rs1085307743 |
Biobank | rs1085307743 |
1000 genomes | rs1085307743 |
hgdp | rs1085307743 |
ensembl | rs1085307743 |
geneview | rs1085307743 |
scholar | rs1085307743 |
rs1085307743 | |
pharmgkb | rs1085307743 |
gwascentral | rs1085307743 |
openSNP | rs1085307743 |
23andMe | rs1085307743 |
SNPshot | rs1085307743 |
SNPdbe | rs1085307743 |
MSV3d | rs1085307743 |
GWAS Ctlg | rs1085307743 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1085307743(-;-) |
Alt | rs1085307743(-;-) |
Reference | Rs1085307743(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CAMTA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.7700576delG |
CLNSRC | |
CLNACC | RCV000488943.1, |