Have questions? Visit https://www.reddit.com/r/SNPedia

rs1800433

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1800433(A;A)
Make rs1800433(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position9079755
GeneA2M
is asnp
is mentioned by
dbSNPrs1800433
ebirs1800433
HLIrs1800433
Exacrs1800433
Varsomers1800433
Maprs1800433
PheGenIrs1800433
hapmaprs1800433
1000 genomesrs1800433
hgdprs1800433
ensemblrs1800433
gopubmedrs1800433
geneviewrs1800433
scholarrs1800433
googlers1800433
pharmgkbrs1800433
gwascentralrs1800433
openSNPrs1800433
23andMers1800433
23andMe allrs1800433
SNP Nexus

SNPshotrs1800433
SNPdbers1800433
MSV3drs1800433
GWAS Ctlgrs1800433
Max Magnitude0
OMIM103950
Desc
Variant0002
Relatedalso
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
CLNACC RCV000019803.2,


[PMID 19105203OA-icon.png] 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.