Have questions? Visit https://www.reddit.com/r/SNPedia

rs774926464

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774926464(C;G)
Make rs774926464(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43060535
GeneCBS
is asnp
is mentioned by
dbSNPrs774926464
ebirs774926464
HLIrs774926464
Exacrs774926464
Varsomers774926464
Maprs774926464
PheGenIrs774926464
hapmaprs774926464
1000 genomesrs774926464
hgdprs774926464
ensemblrs774926464
gopubmedrs774926464
geneviewrs774926464
scholarrs774926464
googlers774926464
pharmgkbrs774926464
gwascentralrs774926464
openSNPrs774926464
23andMers774926464
23andMe allrs774926464
SNP Nexus

SNPshotrs774926464
SNPdbers774926464
MSV3drs774926464
GWAS Ctlgrs774926464
Max Magnitude0
ClinVar
Risk rs774926464(G;G)
Alt rs774926464(G;G)
Reference rs774926464(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44480645C>G
CLNSRC
CLNACC RCV000195902.1,