openSNP

Phenotype: Pseudocholinesterase deficiency

https://en.m.wikipedia.org/wiki/Pseudocholinesterase_deficiency
Inherited blood plasma enzyme abnormality in which the body's production of butyrylcholinesterase (BCHE; pseudocholinesterase) is impaired. People who have this abnormality may be sensitive to certain anesthetic drugs, including the muscle relaxants succinylcholine and mivacurium as well as other ester local anesthetics

Phenotype	Number of Users
Hidradenitis Supperativa	20
CLL	17
Behçet's Syndrome / Disease (Behcet's)	18
lichen planus	16
hemophilia C (factor XI deficiency is caused by "rare mutations" in the F11 gene)	16
Horseshoe kidney	21

User	Variation
Dan	Yes
R-BY86444	Yes
Samantha B. Clark	No
SamBarzilla	No
stephen bradley	No
atelepen	No
Audrey Burns	No and not a carrier rs28933390(G;G)
lms18808	No and not a carrier rs28933390(g;g)
stanto	No and not a carrier rs28933390(g;g)
Whynot	No
Jennifer L. G.	No and not a carrier rs28933390(g;g)
Klevine	No and not a carrier rs28933390(g;g)
Chris1507	No
jderkits	No
jellicoe1992	No
Kaley White	No
owl	No
otis	No
bartlomiejstachera	No and not a carrier rs28933390(g;g)

Known Phenotypes:

Yes
No
No and not a carrier rs28933390(g;g)

Phenotype: Pseudocholinesterase deficiency

Known Phenotypes:

Contacts