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rs769080151

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769080151(A;A)
Make rs769080151(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43060451
GeneCBS
is asnp
is mentioned by
dbSNPrs769080151
ebirs769080151
HLIrs769080151
Exacrs769080151
Varsomers769080151
Maprs769080151
PheGenIrs769080151
hapmaprs769080151
1000 genomesrs769080151
hgdprs769080151
ensemblrs769080151
gopubmedrs769080151
geneviewrs769080151
scholarrs769080151
googlers769080151
pharmgkbrs769080151
gwascentralrs769080151
openSNPrs769080151
23andMers769080151
23andMe allrs769080151
SNP Nexus

SNPshotrs769080151
SNPdbers769080151
MSV3drs769080151
GWAS Ctlgrs769080151
Max Magnitude0
ClinVar
Risk rs769080151(A;A)
Alt rs769080151(A;A)
Reference rs769080151(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44480561G>A
CLNSRC
CLNACC RCV000196320.1,