Talk
Contributions
Create account
Log in
Navigation
SNPedia
Promethease
FAQ
Blog
Recent changes
Random page
Page
Discussion
View form
Edit
History
Have questions? Visit
https://www.reddit.com/r/SNPedia
rs886037611(C;C)
From SNPedia
Jump to:
navigation
,
search
common in clinvar
Is a
genotype
of
rs886037611
Gene
FXN
Chromosome
9
Position
69,035,939
mentioned
by
Magnitude
0
Repute
Good
Geno
Mag
Summary
(-;-)
6
Friedreich's ataxia
(-;C)
3
Carrier of a Friedreich's ataxia mutation
(C;C)
0
common in clinvar
Category
:
Is a genotype
Tools
What links here
Related changes
Special pages
Printable version
Permanent link
Page information
Page values
Browse properties