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rs777919630

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777919630(G;T)
Make rs777919630(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43062358
GeneCBS
is asnp
is mentioned by
dbSNPrs777919630
ebirs777919630
HLIrs777919630
Exacrs777919630
Varsomers777919630
Maprs777919630
PheGenIrs777919630
hapmaprs777919630
1000 genomesrs777919630
hgdprs777919630
ensemblrs777919630
gopubmedrs777919630
geneviewrs777919630
scholarrs777919630
googlers777919630
pharmgkbrs777919630
gwascentralrs777919630
openSNPrs777919630
23andMers777919630
23andMe allrs777919630
SNP Nexus

SNPshotrs777919630
SNPdbers777919630
MSV3drs777919630
GWAS Ctlgrs777919630
Max Magnitude0
ClinVar
Risk rs777919630(T;T)
Alt rs777919630(T;T)
Reference rs777919630(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44482468G>A; NC_000021.8:g.44482468G>T
CLNSRC
CLNACC RCV000173977.3, RCV000199169.1,