rs869025194, RIT1

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Noonan Syndrome
CUI: C0028326
Disease: Noonan Syndrome
187 0.882 0.280 1 155904496 missense variant A/C;G;T snv 0.710 1.000 1 2016 2016
NOONAN SYNDROME 8
CUI: C3809233
Disease: NOONAN SYNDROME 8
12 0.882 0.280 1 155904496 missense variant A/C;G;T snv 0.700 1.000 7 2013 2016
Cancer of Urinary Tract
CUI: C0751571
Disease: Cancer of Urinary Tract
11 0.882 0.280 1 155904496 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.882 0.280 1 155904496 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016