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rs140002610

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs140002610(A;A)
Make rs140002610(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43066300
GeneCBS
is asnp
is mentioned by
dbSNPrs140002610
ebirs140002610
HLIrs140002610
Exacrs140002610
Varsomers140002610
Maprs140002610
PheGenIrs140002610
hapmaprs140002610
1000 genomesrs140002610
hgdprs140002610
ensemblrs140002610
gopubmedrs140002610
geneviewrs140002610
scholarrs140002610
googlers140002610
pharmgkbrs140002610
gwascentralrs140002610
openSNPrs140002610
23andMers140002610
23andMe allrs140002610
SNP Nexus

SNPshotrs140002610
SNPdbers140002610
MSV3drs140002610
GWAS Ctlgrs140002610
Max Magnitude0
ClinVar
Risk rs140002610(A;A)
Alt rs140002610(A;A)
Reference rs140002610(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene CBS
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.44486410G>A
CLNSRC
CLNACC RCV000195820.2,