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rs762341786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762341786(G;T)
Make rs762341786(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position165829750
GeneBCHE
is asnp
is mentioned by
dbSNPrs762341786
dbSNP (classic)rs762341786
ClinGenrs762341786
ebirs762341786
HLIrs762341786
Exacrs762341786
Gnomadrs762341786
Varsomers762341786
LitVarrs762341786
Maprs762341786
PheGenIrs762341786
Biobankrs762341786
1000 genomesrs762341786
hgdprs762341786
ensemblrs762341786
geneviewrs762341786
scholarrs762341786
googlers762341786
pharmgkbrs762341786
gwascentralrs762341786
openSNPrs762341786
23andMers762341786
23andMe allrs762341786
SNPshotrs762341786
SNPdbers762341786
MSV3drs762341786
GWAS Ctlgrs762341786
Max Magnitude0
ClinVar
Risk rs762341786(C;C) rs762341786(T;T)
Alt rs762341786(C;C) rs762341786(T;T)
Reference Rs762341786(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.165547538G>T
CLNSRC
CLNACC RCV000409122.1,