rs1085308017
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Chromosome | 18 |
Position | 23914539 |
Gene | LAMA3 |
is a | snp |
is | mentioned by |
dbSNP | rs1085308017 |
dbSNP (classic) | rs1085308017 |
ClinGen | rs1085308017 |
ebi | rs1085308017 |
HLI | rs1085308017 |
Exac | rs1085308017 |
Gnomad | rs1085308017 |
Varsome | rs1085308017 |
LitVar | rs1085308017 |
Map | rs1085308017 |
PheGenI | rs1085308017 |
Biobank | rs1085308017 |
1000 genomes | rs1085308017 |
hgdp | rs1085308017 |
ensembl | rs1085308017 |
geneview | rs1085308017 |
scholar | rs1085308017 |
rs1085308017 | |
pharmgkb | rs1085308017 |
gwascentral | rs1085308017 |
openSNP | rs1085308017 |
23andMe | rs1085308017 |
SNPshot | rs1085308017 |
SNPdbe | rs1085308017 |
MSV3d | rs1085308017 |
GWAS Ctlg | rs1085308017 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1085308017(T;T) |
Alt | rs1085308017(T;T) |
Reference | Rs1085308017(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LAMA3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.21494503A>T |
CLNSRC | |
CLNACC | RCV000489231.1, |