Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11001553
rs11001553
0.925 0.080 10 52313141 intron variant C/T snv 0.12
CUI: C0020608
Disease: Hypodontia
Hypodontia
0.020 1.000 2 2012 2014
dbSNP: rs10824310
rs10824310
1.000 0.080 10 52268704 intron variant C/T snv 4.7E-02
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.010 1.000 1 2017 2017
dbSNP: rs11001553
rs11001553
0.925 0.080 10 52313141 intron variant C/T snv 0.12
CUI: C0000846
Disease: Agenesis
Agenesis
0.010 1.000 1 2014 2014
dbSNP: rs145640971
rs145640971
1.000 0.040 10 52314555 missense variant G/A snv 1.3E-04 1.3E-04
CUI: C0079218
Disease: Fibromatosis, Aggressive
Fibromatosis, Aggressive
0.010 1.000 1 2019 2019
dbSNP: rs149268042
rs149268042
1.000 0.040 10 52315038 missense variant G/T snv 2.9E-03 2.6E-03
CUI: C0029401
Disease: Osteitis Deformans
Osteitis Deformans
0.010 1.000 1 2013 2013
dbSNP: rs1896368
rs1896368
1.000 0.040 10 52309144 intron variant C/T snv 0.43
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.010 1.000 1 2020 2020