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rs745704046

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745704046(C;T)
Make rs745704046(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43065690
GeneCBS
is asnp
is mentioned by
dbSNPrs745704046
ebirs745704046
HLIrs745704046
Exacrs745704046
Varsomers745704046
Maprs745704046
PheGenIrs745704046
hapmaprs745704046
1000 genomesrs745704046
hgdprs745704046
ensemblrs745704046
gopubmedrs745704046
geneviewrs745704046
scholarrs745704046
googlers745704046
pharmgkbrs745704046
gwascentralrs745704046
openSNPrs745704046
23andMers745704046
23andMe allrs745704046
SNP Nexus

SNPshotrs745704046
SNPdbers745704046
MSV3drs745704046
GWAS Ctlgrs745704046
Max Magnitude0
ClinVar
Risk rs745704046(T;T)
Alt rs745704046(T;T)
Reference rs745704046(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44485800C>T
CLNSRC
CLNACC RCV000195644.1,