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rs746332433

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746332433(C;C)
Make rs746332433(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position109627794
GeneAMPD2
is asnp
is mentioned by
dbSNPrs746332433
ebirs746332433
HLIrs746332433
Exacrs746332433
Varsomers746332433
Maprs746332433
PheGenIrs746332433
hapmaprs746332433
1000 genomesrs746332433
hgdprs746332433
ensemblrs746332433
gopubmedrs746332433
geneviewrs746332433
scholarrs746332433
googlers746332433
pharmgkbrs746332433
gwascentralrs746332433
openSNPrs746332433
23andMers746332433
23andMe allrs746332433
SNP Nexus

SNPshotrs746332433
SNPdbers746332433
MSV3drs746332433
GWAS Ctlgrs746332433
Max Magnitude0
ClinVar
Risk rs746332433(C;C)
Alt rs746332433(C;C)
Reference rs746332433(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene AMPD2
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.110170416G>C
CLNSRC
CLNACC RCV000210593.1,