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rs863223434

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223434(C;T)
Make rs863223434(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43058912
GeneCBS
is asnp
is mentioned by
dbSNPrs863223434
ebirs863223434
HLIrs863223434
Exacrs863223434
Varsomers863223434
Maprs863223434
PheGenIrs863223434
hapmaprs863223434
1000 genomesrs863223434
hgdprs863223434
ensemblrs863223434
gopubmedrs863223434
geneviewrs863223434
scholarrs863223434
googlers863223434
pharmgkbrs863223434
gwascentralrs863223434
openSNPrs863223434
23andMers863223434
23andMe allrs863223434
SNP Nexus

SNPshotrs863223434
SNPdbers863223434
MSV3drs863223434
GWAS Ctlgrs863223434
Max Magnitude0
ClinVar
Risk rs863223434(T;T)
Alt rs863223434(T;T)
Reference rs863223434(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.44479022G>A
CLNSRC
CLNACC RCV000197292.1,