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rs1789953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1789953(C;T)
Make rs1789953(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome21
Position43062826
GeneCBS
is asnp
is mentioned by
dbSNPrs1789953
dbSNP (classic)rs1789953
ClinGenrs1789953
ebirs1789953
HLIrs1789953
Exacrs1789953
Gnomadrs1789953
Varsomers1789953
LitVarrs1789953
Maprs1789953
PheGenIrs1789953
Biobankrs1789953
1000 genomesrs1789953
hgdprs1789953
ensemblrs1789953
geneviewrs1789953
scholarrs1789953
googlers1789953
pharmgkbrs1789953
gwascentralrs1789953
openSNPrs1789953
23andMers1789953
SNPshotrs1789953
SNPdbers1789953
MSV3drs1789953
GWAS Ctlgrs1789953
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 26955774] The association of single nucleotide polymorphisms of the maternal cystathionine-β-synthase gene with early-onset preeclampsia.

ClinVar
Risk rs1789953(T;T)
Alt rs1789953(T;T)
Reference Rs1789953(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CBSL CBS
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.44482936C>T
CLNSRC
CLNACC RCV000198954.1,