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rs28934892

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs28934892(C;T)
Make rs28934892(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position43058927
GeneCBS
is asnp
is mentioned by
dbSNPrs28934892
ebirs28934892
HLIrs28934892
Exacrs28934892
Varsomers28934892
Maprs28934892
PheGenIrs28934892
hapmaprs28934892
1000 genomesrs28934892
hgdprs28934892
ensemblrs28934892
gopubmedrs28934892
geneviewrs28934892
scholarrs28934892
googlers28934892
pharmgkbrs28934892
gwascentralrs28934892
openSNPrs28934892
23andMers28934892
23andMe allrs28934892
SNP Nexus

SNPshotrs28934892
SNPdbers28934892
MSV3drs28934892
GWAS Ctlgrs28934892
Max Magnitude0
OMIM236200
DescTHROMBOSIS, HYPERHOMOCYSTEINEMIC
Variant0013
Relatedalso
Neighborrs28934275
Distance5004
Neighborrs28934891
Distance65
OMIM613381
Desc
Variant0013
Relatedalso


ClinVar
Risk rs28934892(T;T)
Alt rs28934892(T;T)
Reference rs28934892(C;C)
Significance Pathogenic
Disease HYPERHOMOCYSTEINEMIA
Variation info
Gene CBS
CLNDBN HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED
Reversed 1
HGVS NC_000021.8:g.44479037G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000152.2,