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rs863223435

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223435(A;A)
Make rs863223435(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43068572
GeneCBS
is asnp
is mentioned by
dbSNPrs863223435
ebirs863223435
HLIrs863223435
Exacrs863223435
Varsomers863223435
Maprs863223435
PheGenIrs863223435
hapmaprs863223435
1000 genomesrs863223435
hgdprs863223435
ensemblrs863223435
gopubmedrs863223435
geneviewrs863223435
scholarrs863223435
googlers863223435
pharmgkbrs863223435
gwascentralrs863223435
openSNPrs863223435
23andMers863223435
23andMe allrs863223435
SNP Nexus

SNPshotrs863223435
SNPdbers863223435
MSV3drs863223435
GWAS Ctlgrs863223435
Max Magnitude0
ClinVar
Risk rs863223435(A;A)
Alt rs863223435(A;A)
Reference rs863223435(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.44488682C>T
CLNSRC
CLNACC RCV000195506.1,