Source: GWASDB

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: rs1231206
rs1231206
SMG6
1.000 0.040 17 2222311 intron variant G/A snv 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2011
dbSNP: rs17761864
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.800 1.000 1 2012 2012
dbSNP: rs216172
rs216172
SMG6
0.925 0.040 17 2223210 intron variant G/C snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2011
dbSNP: rs4523957
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2013 2019
dbSNP: rs2281727
rs2281727
SMG6
0.882 0.080 17 2214651 intron variant A/G snv 0.38
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0.700 1.000 1 2013 2013
dbSNP: rs2281727
rs2281727
SMG6
0.882 0.080 17 2214651 intron variant A/G snv 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2014 2014
dbSNP: rs4790881
rs4790881
SMG6
17 2165638 intron variant C/A snv 0.75
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2012 2012