Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11431
rs11431
14 54788955 3 prime UTR variant C/A;G;T snv 1.2E-05; 0.53
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement
0.700 1.000 1 2018 2018
dbSNP: rs11624106
rs11624106
14 54713435 intron variant A/G snv 0.16
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement
0.700 1.000 1 2018 2018
dbSNP: rs4901536
rs4901536
0.925 0.080 14 54733816 intron variant T/C snv 0.67
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4901536
rs4901536
0.925 0.080 14 54733816 intron variant T/C snv 0.67
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs4901541
rs4901541
14 54768564 intron variant C/T snv 0.49
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs709939
rs709939
14 54782627 intron variant C/T snv 0.55
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2011 2011
dbSNP: rs7147275
rs7147275
14 54766806 intron variant G/A snv 0.16
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement
0.700 1.000 1 2018 2018
dbSNP: rs7156787
rs7156787
14 54734963 non coding transcript exon variant A/G;T snv
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs7156891
rs7156891
14 54734789 intron variant G/A snv 0.80
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1957358
rs1957358
1.000 0.080 14 54755757 intron variant T/A;C snv
CUI: C0149744
Disease: Oral lesion
Oral lesion
Digestive System Diseases; Stomatognathic Diseases 0.700 0
dbSNP: rs1957358
rs1957358
1.000 0.080 14 54755757 intron variant T/A;C snv
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.700 0