rs778568717

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs778568717(-;-)

Make rs778568717(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

165830241

Gene

BCHE

is a	snp
is	mentioned by
dbSNP	rs778568717
dbSNP (classic)	rs778568717
ClinGen	rs778568717
ebi	rs778568717
HLI	rs778568717
Exac	rs778568717
Gnomad	rs778568717
Varsome	rs778568717
LitVar	rs778568717
Map	rs778568717
PheGenI	rs778568717
Biobank	rs778568717
1000 genomes	rs778568717
hgdp	rs778568717
ensembl	rs778568717
geneview	rs778568717
scholar	rs778568717
google	rs778568717
pharmgkb	rs778568717
gwascentral	rs778568717
openSNP	rs778568717
23andMe	rs778568717
SNPshot	rs778568717
SNPdbe	rs778568717
MSV3d	rs778568717
GWAS Ctlg	rs778568717

Max Magnitude

0

ClinVar
Risk	rs778568717(-;-)
Alt	rs778568717(-;-)
Reference	Rs778568717(A;A)
Significance	Probable-Pathogenic
Disease	Deficiency of butyrylcholine esterase
Variation	info
Gene	BCHE
CLNDBN	Deficiency of butyrylcholine esterase
Reversed	0
HGVS	NC_000003.11:g.165548029delA
CLNSRC
CLNACC	RCV000410837.1,