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rs863223430

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223430(G;G)
Make rs863223430(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43065201
GeneCBS
is asnp
is mentioned by
dbSNPrs863223430
ebirs863223430
HLIrs863223430
Exacrs863223430
Varsomers863223430
Maprs863223430
PheGenIrs863223430
hapmaprs863223430
1000 genomesrs863223430
hgdprs863223430
ensemblrs863223430
gopubmedrs863223430
geneviewrs863223430
scholarrs863223430
googlers863223430
pharmgkbrs863223430
gwascentralrs863223430
openSNPrs863223430
23andMers863223430
23andMe allrs863223430
SNP Nexus

SNPshotrs863223430
SNPdbers863223430
MSV3drs863223430
GWAS Ctlgrs863223430
Max Magnitude0
ClinVar
Risk rs863223430(G;G)
Alt rs863223430(G;G)
Reference rs863223430(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.44485311A>C
CLNSRC
CLNACC RCV000196686.1,