rs4498834, CACNA1S

N. diseases: 8
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.
Developmental absence of tooth
CUI: C0399352
Disease: Developmental absence of tooth
15 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
Hypodontia
CUI: C0020608
Disease: Hypodontia
48 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
Hypodontia Oligodontia with Orofacial Cleft
8 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
Oligodontia
CUI: C4082304
Disease: Oligodontia
34 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
Tooth Agenesis, Familial
CUI: C3489529
Disease: Tooth Agenesis, Familial
13 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
TOOTH AGENESIS, SELECTIVE, 9
CUI: C4310638
Disease: TOOTH AGENESIS, SELECTIVE, 9
11 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
Tooth Agenesis, Selective, With Orofacial Cleft
8 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
Tooth development and eruption disorder
8 0.776 0.160 1 201111170 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018