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rs760182781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760182781(A;A)
Make rs760182781(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position165830595
GeneBCHE
is asnp
is mentioned by
dbSNPrs760182781
dbSNP (classic)rs760182781
ClinGenrs760182781
ebirs760182781
HLIrs760182781
Exacrs760182781
Gnomadrs760182781
Varsomers760182781
LitVarrs760182781
Maprs760182781
PheGenIrs760182781
Biobankrs760182781
1000 genomesrs760182781
hgdprs760182781
ensemblrs760182781
geneviewrs760182781
scholarrs760182781
googlers760182781
pharmgkbrs760182781
gwascentralrs760182781
openSNPrs760182781
23andMers760182781
23andMe allrs760182781
SNPshotrs760182781
SNPdbers760182781
MSV3drs760182781
GWAS Ctlgrs760182781
Max Magnitude0
ClinVar
Risk rs760182781(A;A) rs760182781(C;C)
Alt rs760182781(A;A) rs760182781(C;C)
Reference Rs760182781(G;G)
Significance Probable-Pathogenic
Disease Deficiency of butyrylcholine esterase
Variation info
Gene BCHE
CLNDBN Deficiency of butyrylcholine esterase
Reversed 0
HGVS NC_000003.11:g.165548383G>A
CLNSRC
CLNACC RCV000409468.1,