Source: CURATED

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: rs3204689
rs3204689
ALDH1A2
1.000 0.040 15 57954604 3 prime UTR variant G/C snv 0.37
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.700 1.000 1 2014 2014
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		0.710 1.000 1 2013 2015
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases 		0.700 1.000 1 2013 2013
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0012242
Disease: Digestive System Disorders
Digestive System Disorders 		0.700 1.000 1 2013 2013
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0021831
Disease: Intestinal Diseases
Intestinal Diseases 		0.700 1.000 1 2013 2013
dbSNP: rs3784262
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.820 0.667 1 2013 2016
dbSNP: rs66725070
rs66725070
ALDH1A2
1.000 0.080 15 57975219 intron variant ACAT/- delins 0.35
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.700 1.000 1 2016 2016
dbSNP: rs11635486
rs11635486
ALDH1A2 ; LOC283665
15 58068926 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2464469
rs2464469
ALDH1A2 ; LOC283665
0.925 0.080 15 58069827 intron variant G/A snv 0.65
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		0.700 1.000 1 2016 2016
dbSNP: rs2464469
rs2464469
ALDH1A2 ; LOC283665
0.925 0.080 15 58069827 intron variant G/A snv 0.65
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.700 1.000 1 2016 2016
dbSNP: rs16953360
rs16953360
AQP9 ; ALDH1A2
15 58155995 non coding transcript exon variant A/G snv 2.3E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12441883
rs12441883
AQP9 ; ALDH1A2
15 58164651 intron variant G/A snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2280195
rs2280195
AQP9 ; ALDH1A2
15 58174896 intron variant G/A snv 0.37 0.40
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs16939881
rs16939881
AQP9 ; ALDH1A2
15 58179780 intron variant G/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16939881
rs16939881
AQP9 ; ALDH1A2
15 58179780 intron variant G/C;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2012 2012
dbSNP: rs2077737
rs2077737
ALDH1A2
15 58186751 intron variant T/C snv 0.25
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12900815
rs12900815
ALDH1A2
15 58193483 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11857136
rs11857136
ALDH1A2
15 58208580 intron variant T/A snv 0.61
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs56227417
rs56227417
ALDH1A2
15 58208757 intron variant T/C snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4350519
rs4350519
ALDH1A2
15 58208947 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1618701
rs1618701
ALDH1A2
15 58209083 intron variant T/A snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7180071
rs7180071
ALDH1A2
15 58210273 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2414551
rs2414551
ALDH1A2
15 58210929 intron variant T/C snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1663253
rs1663253
ALDH1A2
15 58212479 intron variant C/T snv 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2017566
rs2017566
ALDH1A2
15 58212841 intron variant T/C snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012