rs1557962794, 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 8
CUI: C3809233
Disease: NOONAN SYNDROME 8
12 0.882 0.160 1 155910693 missense variant T/G snv 0.700 1.000 1 2016 2016
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.882 0.160 1 155910693 missense variant T/G snv 0.700 0
Noonan Syndrome 1
CUI: C4551602
Disease: Noonan Syndrome 1
83 0.882 0.160 1 155910693 missense variant T/G snv 0.700 0
Pulmonary Stenosis
CUI: C1956257
Disease: Pulmonary Stenosis
40 0.882 0.160 1 155910693 missense variant T/G snv 0.700 0