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

rs121918556

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918556(A;T)
Make rs121918556(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position165786255
GeneBCHE
is asnp
is mentioned by
dbSNPrs121918556
ebirs121918556
HLIrs121918556
Exacrs121918556
Varsomers121918556
Maprs121918556
PheGenIrs121918556
hapmaprs121918556
1000 genomesrs121918556
hgdprs121918556
ensemblrs121918556
gopubmedrs121918556
geneviewrs121918556
scholarrs121918556
googlers121918556
pharmgkbrs121918556
gwascentralrs121918556
openSNPrs121918556
23andMers121918556
23andMe allrs121918556
SNP Nexus

SNPshotrs121918556
SNPdbers121918556
MSV3drs121918556
GWAS Ctlgrs121918556
Max Magnitude0
OMIM177400
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918556(T;T)
Alt rs121918556(T;T)
Reference rs121918556(A;A)
Significance Pathogenic
Disease Bche
Variation info
Gene BCHE
CLNDBN Bche, j variant Bche, quantitative j variant
Reversed 1
HGVS NC_000003.11:g.165504043T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014124.23, RCV000014125.23,