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rs1800434

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1800434(A;A)
Make rs1800434(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position9094987
GeneA2M
is asnp
is mentioned by
dbSNPrs1800434
ebirs1800434
HLIrs1800434
Exacrs1800434
Varsomers1800434
Maprs1800434
PheGenIrs1800434
hapmaprs1800434
1000 genomesrs1800434
hgdprs1800434
ensemblrs1800434
gopubmedrs1800434
geneviewrs1800434
scholarrs1800434
googlers1800434
pharmgkbrs1800434
gwascentralrs1800434
openSNPrs1800434
23andMers1800434
23andMe allrs1800434
SNP Nexus

SNPshotrs1800434
SNPdbers1800434
MSV3drs1800434
GWAS Ctlgrs1800434
Max Magnitude0
OMIM103950
Desc
Variant0004
Relatedalso
ClinVar
Risk rs1800434(A;A)
Alt rs1800434(A;A)
Reference rs1800434(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.9247583C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019805.2,