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rs869312928

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312928(A;G)
Make rs869312928(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position109627893
GeneAMPD2
is asnp
is mentioned by
dbSNPrs869312928
ebirs869312928
HLIrs869312928
Exacrs869312928
Varsomers869312928
Maprs869312928
PheGenIrs869312928
hapmaprs869312928
1000 genomesrs869312928
hgdprs869312928
ensemblrs869312928
gopubmedrs869312928
geneviewrs869312928
scholarrs869312928
googlers869312928
pharmgkbrs869312928
gwascentralrs869312928
openSNPrs869312928
23andMers869312928
23andMe allrs869312928
SNP Nexus

SNPshotrs869312928
SNPdbers869312928
MSV3drs869312928
GWAS Ctlgrs869312928
Max Magnitude0
ClinVar
Risk rs869312928(G;G)
Alt rs869312928(G;G)
Reference rs869312928(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene AMPD2
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.110170515A>G
CLNSRC
CLNACC RCV000210639.1,