DAGLA, diacylglycerol lipase alpha, 747

N. diseases: 19; N. variants: 47
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: rs10488693
rs10488693
11 61717684 intron variant C/T snv 6.0E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs10488693
rs10488693
11 61717684 intron variant C/T snv 6.0E-02
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs11230781
rs11230781
11 61682858 intron variant G/A snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11827215
rs11827215
11 61691123 intron variant G/A snv 0.13
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11828739
rs11828739
11 61740602 intron variant C/T snv 0.22 0.20
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12274157
rs12274157
11 61710175 intron variant A/C snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12285167
rs12285167
11 61724567 intron variant C/A snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17156244
rs17156244
11 61714923 intron variant T/G snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17156254
rs17156254
11 61722773 intron variant G/A snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs17827918
rs17827918
11 61700693 intron variant G/A;T snv 9.0E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198426
rs198426
11 61723014 intron variant C/T snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs198428
rs198428
11 61722233 intron variant A/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs198435
rs198435
11 61715852 intron variant G/C snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198437
rs198437
11 61711850 intron variant G/A snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198442
rs198442
11 61738996 intron variant C/A;T snv 0.43
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs198442
rs198442
11 61738996 intron variant C/A;T snv 0.43
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198443
rs198443
11 61738224 intron variant G/T snv 0.46 0.43
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198444
rs198444
11 61737696 synonymous variant G/A snv 0.46 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198447
rs198447
11 61734120 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198448
rs198448
11 61733015 intron variant C/T snv 0.40
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198452
rs198452
11 61700131 intron variant G/A snv 0.40
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs198457
rs198457
1.000 0.040 11 61704206 intron variant C/T snv 0.12
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs2003019
rs2003019
11 61707995 intron variant T/G snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2013326
rs2013326
11 61733804 intron variant G/A snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs2014094
rs2014094
11 61746480 3 prime UTR variant G/A snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012