rs1800433
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1800433(A;A) |
Make rs1800433(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 9079755 |
Gene | A2M, KLRG1 |
is a | snp |
is | mentioned by |
dbSNP | rs1800433 |
dbSNP (classic) | rs1800433 |
ClinGen | rs1800433 |
ebi | rs1800433 |
HLI | rs1800433 |
Exac | rs1800433 |
Gnomad | rs1800433 |
Varsome | rs1800433 |
LitVar | rs1800433 |
Map | rs1800433 |
PheGenI | rs1800433 |
Biobank | rs1800433 |
1000 genomes | rs1800433 |
hgdp | rs1800433 |
ensembl | rs1800433 |
geneview | rs1800433 |
scholar | rs1800433 |
rs1800433 | |
pharmgkb | rs1800433 |
gwascentral | rs1800433 |
openSNP | rs1800433 |
23andMe | rs1800433 |
SNPshot | rs1800433 |
SNPdbe | rs1800433 |
MSV3d | rs1800433 |
GWAS Ctlg | rs1800433 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1800433(A;A) |
Alt | rs1800433(A;A) |
Reference | Rs1800433(G;G) |
Significance | Non-pathogenic |
Disease | ALPHA-2-MACROGLOBULIN POLYMORPHISM |
Variation | info |
Gene | A2M |
CLNDBN | ALPHA-2-MACROGLOBULIN POLYMORPHISM |
Reversed | 1 |
HGVS | NC_000012.11:g.9232351C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019803.2, |
[PMID 19105203] An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.