rs706895

Orientation

plus

Stabilized

plus

Make rs706895(C;C)

Make rs706895(C;T)

Make rs706895(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

111720156

Gene

FYN

is a	snp
is	mentioned by
dbSNP	rs706895
dbSNP (classic)	rs706895
ClinGen	rs706895
ebi	rs706895
HLI	rs706895
Exac	rs706895
Gnomad	rs706895
Varsome	rs706895
LitVar	rs706895
Map	rs706895
PheGenI	rs706895
Biobank	rs706895
1000 genomes	rs706895
hgdp	rs706895
ensembl	rs706895
geneview	rs706895
scholar	rs706895
google	rs706895
pharmgkb	rs706895
gwascentral	rs706895
openSNP	rs706895
23andMe	rs706895
SNPshot	rs706895
SNPdbe	rs706895
MSV3d	rs706895
GWAS Ctlg	rs706895

GMAF

0.4206

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 19468241] Functional impact of endotoxin receptor CD14 polymorphisms on transcriptional activity

[PMID 21207251] Fyn Polymorphisms are Associated with Distinct Personality Traits in Healthy Chinese-Han Subjects

The rs706895C/T polymorphism of FYN is associated with the variance in harm avoidance (HA2: fear of uncertainty, reduced in C/T vs TT) and reward dependence (RD1: sentimentality,reduced in CC homozygotes vs CT) behaviors in healthy Chinese-Han subjects.

[PMID 26407913] Role of the Fyn -93A>G polymorphism (rs706895) in acute rejection after liver transplantation