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rs372010465

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372010465(C;T)
Make rs372010465(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43060475
GeneCBS
is asnp
is mentioned by
dbSNPrs372010465
ebirs372010465
HLIrs372010465
Exacrs372010465
Varsomers372010465
Maprs372010465
PheGenIrs372010465
hapmaprs372010465
1000 genomesrs372010465
hgdprs372010465
ensemblrs372010465
gopubmedrs372010465
geneviewrs372010465
scholarrs372010465
googlers372010465
pharmgkbrs372010465
gwascentralrs372010465
openSNPrs372010465
23andMers372010465
23andMe allrs372010465
SNP Nexus

SNPshotrs372010465
SNPdbers372010465
MSV3drs372010465
GWAS Ctlgrs372010465
Max Magnitude0
ClinVar
Risk rs372010465(T;T)
Alt rs372010465(T;T)
Reference rs372010465(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44480585C>T
CLNSRC
CLNACC RCV000196393.1,