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rs3495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3495(A;A)
Make rs3495(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position165773193
GeneBCHE
is asnp
is mentioned by
dbSNPrs3495
dbSNP (old)rs3495
ClinGenrs3495
ebirs3495
HLIrs3495
Exacrs3495
Gnomadrs3495
Varsomers3495
Maprs3495
PheGenIrs3495
Biobankrs3495
1000 genomesrs3495
hgdprs3495
ensemblrs3495
gopubmedrs3495
geneviewrs3495
scholarrs3495
googlers3495
pharmgkbrs3495
gwascentralrs3495
openSNPrs3495
23andMers3495
23andMe allrs3495
SNP Nexus

SNPshotrs3495
SNPdbers3495
MSV3drs3495
GWAS Ctlgrs3495
GMAF0.3329
Max Magnitude0

[PMID 21547979] Variability of the BCHE gene in Amerindians from Paraná, Brazil


ClinVar
Risk rs3495(A;A)
Alt rs3495(A;A)
Reference Rs3495(G;G)
Significance Non-pathogenic
Disease Deficiency of butyrylcholine esterase
Variation info
Gene BCHE
CLNDBN Deficiency of butyrylcholine esterase
Reversed 1
HGVS NC_000003.11:g.165490981C>T
CLNSRC
CLNACC RCV000374138.1,