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rs863223436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGGCGGTGG;TGGCGGTGG) 0 common in clinvar
Make rs863223436(-;-)
Make rs863223436(-;TGGCGGTGG)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43060517
GeneCBS
is asnp
is mentioned by
dbSNPrs863223436
dbSNP (old)rs863223436
ClinGenrs863223436
ebirs863223436
HLIrs863223436
Exacrs863223436
Gnomadrs863223436
Varsomers863223436
Maprs863223436
PheGenIrs863223436
Biobankrs863223436
1000 genomesrs863223436
hgdprs863223436
ensemblrs863223436
gopubmedrs863223436
geneviewrs863223436
scholarrs863223436
googlers863223436
pharmgkbrs863223436
gwascentralrs863223436
openSNPrs863223436
23andMers863223436
23andMe allrs863223436
SNP Nexus

SNPshotrs863223436
SNPdbers863223436
MSV3drs863223436
GWAS Ctlgrs863223436
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs863223436(TGGCGGTGG;TGGCGGTGG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.44480627_44480635delCCACCGCCA
CLNSRC
CLNACC RCV000195988.1,