rs200288072
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs200288072(A;A) |
Make rs200288072(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 129050089 |
Gene | LAMA2 |
is a | snp |
is | mentioned by |
dbSNP | rs200288072 |
dbSNP (classic) | rs200288072 |
ClinGen | rs200288072 |
ebi | rs200288072 |
HLI | rs200288072 |
Exac | rs200288072 |
Gnomad | rs200288072 |
Varsome | rs200288072 |
LitVar | rs200288072 |
Map | rs200288072 |
PheGenI | rs200288072 |
Biobank | rs200288072 |
1000 genomes | rs200288072 |
hgdp | rs200288072 |
ensembl | rs200288072 |
geneview | rs200288072 |
scholar | rs200288072 |
rs200288072 | |
pharmgkb | rs200288072 |
gwascentral | rs200288072 |
openSNP | rs200288072 |
23andMe | rs200288072 |
SNPshot | rs200288072 |
SNPdbe | rs200288072 |
MSV3d | rs200288072 |
GWAS Ctlg | rs200288072 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200288072(A;A) |
Alt | rs200288072(A;A) |
Reference | Rs200288072(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | LAMA2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.129371234G>A |
CLNSRC | |
CLNACC | RCV000444644.1, |