English
Talk
Contributions
Create account
Log in
Toggle navigation
Navigation
SNPedia
Promethease
FAQ
Blog
Recent changes
Random page
Page
Discussion
Edit with form
Edit
History
Have questions? Visit
https://www.reddit.com/r/SNPedia
rs104894402(C;T)
From SNPedia
(Redirected from
I5001995(A;G)
)
Jump to:
navigation
,
search
Deafness mutation (dominant)
Is a
genotype
of
rs104894402
Gene
GJB2
Chromosome
13
Position
20,189,359
mentioned
by
Magnitude
4
Repute
Bad
Geno
Mag
Summary
(C;C)
0
common in clinvar
(C;T)
4
Deafness mutation (dominant)
see
GJB2
and
deafness
Category
:
Is a genotype
What links here
Related changes
Special pages
Printable version
Permanent link
Page information
Page values
Browse properties
This page was last edited on 29 June 2016, at 00:13.
Privacy policy
About SNPedia
Disclaimers