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rs398124629

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124629(A;G)
Make rs398124629(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position66228149
GeneAPOH
is asnp
is mentioned by
dbSNPrs398124629
ebirs398124629
HLIrs398124629
Exacrs398124629
Varsomers398124629
Maprs398124629
PheGenIrs398124629
hapmaprs398124629
1000 genomesrs398124629
hgdprs398124629
ensemblrs398124629
gopubmedrs398124629
geneviewrs398124629
scholarrs398124629
googlers398124629
pharmgkbrs398124629
gwascentralrs398124629
openSNPrs398124629
23andMers398124629
23andMe allrs398124629
SNP Nexus

SNPshotrs398124629
SNPdbers398124629
MSV3drs398124629
GWAS Ctlgrs398124629
Max Magnitude0
ClinVar
Risk rs398124629(G;G)
Alt rs398124629(G;G)
Reference rs398124629(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APOH
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.64224267T>C
CLNSRC ClinVar
CLNACC RCV000082872.1,