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rs772450760

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs772450760(A;T)
Make rs772450760(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43068559
GeneCBS
is asnp
is mentioned by
dbSNPrs772450760
ebirs772450760
HLIrs772450760
Exacrs772450760
Varsomers772450760
Maprs772450760
PheGenIrs772450760
hapmaprs772450760
1000 genomesrs772450760
hgdprs772450760
ensemblrs772450760
gopubmedrs772450760
geneviewrs772450760
scholarrs772450760
googlers772450760
pharmgkbrs772450760
gwascentralrs772450760
openSNPrs772450760
23andMers772450760
23andMe allrs772450760
SNP Nexus

SNPshotrs772450760
SNPdbers772450760
MSV3drs772450760
GWAS Ctlgrs772450760
Max Magnitude0
ClinVar
Risk rs772450760(T;T)
Alt rs772450760(T;T)
Reference rs772450760(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44488669A>T
CLNSRC
CLNACC RCV000197745.1,