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rs121964970

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964970(A;A)
Make rs121964970(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position43065645
GeneCBS
is asnp
is mentioned by
dbSNPrs121964970
ebirs121964970
HLIrs121964970
Exacrs121964970
Varsomers121964970
Maprs121964970
PheGenIrs121964970
hapmaprs121964970
1000 genomesrs121964970
hgdprs121964970
ensemblrs121964970
gopubmedrs121964970
geneviewrs121964970
scholarrs121964970
googlers121964970
pharmgkbrs121964970
gwascentralrs121964970
openSNPrs121964970
23andMers121964970
23andMe allrs121964970
SNP Nexus

SNPshotrs121964970
SNPdbers121964970
MSV3drs121964970
GWAS Ctlgrs121964970
Max Magnitude0
OMIM613381
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121964970(A;A)
Alt rs121964970(A;A)
Reference rs121964970(G;G)
Significance Other
Disease Homocystinuria not provided
Variation info
Gene CBS
CLNDBN Homocystinuria, pyridoxine-responsive not provided
Reversed 1
HGVS NC_000021.8:g.44485755C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000150.2, RCV000179250.2,