Source: ALL

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: rs724016
rs724016
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 6 2008 2019
dbSNP: rs6440003
rs6440003
3 141375367 intron variant G/A snv 0.54
CUI: C0489786
Disease: Height
Height
0.700 1.000 4 2008 2011
dbSNP: rs6763931
rs6763931
0.925 0.080 3 141383991 intron variant G/A snv 0.54
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2008 2019
dbSNP: rs724016
rs724016
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52
CUI: C0489786
Disease: Height
Height
0.700 1.000 4 2008 2011
dbSNP: rs1991431
rs1991431
3 141414608 intron variant G/A snv 0.50
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 3 2013 2019
dbSNP: rs6440003
rs6440003
3 141375367 intron variant G/A snv 0.54
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 3 2008 2019
dbSNP: rs6763931
rs6763931
0.925 0.080 3 141383991 intron variant G/A snv 0.54
CUI: C0489786
Disease: Height
Height
0.700 1.000 3 2008 2011
dbSNP: rs10513137
rs10513137
3 141424588 intron variant G/A;C snv
CUI: C0489786
Disease: Height
Height
0.700 1.000 2 2009 2010
dbSNP: rs10513137
rs10513137
3 141424588 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2009 2010
dbSNP: rs6763931
rs6763931
0.925 0.080 3 141383991 intron variant G/A snv 0.54
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.700 1.000 2 2011 2018
dbSNP: rs114097136
rs114097136
3 141395171 intron variant C/G snv 3.6E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs1344672
rs1344672
3 141406863 intron variant C/G snv 0.55
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs1344674
rs1344674
3 141406344 intron variant A/G snv 0.55
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1344674
rs1344674
3 141406344 intron variant A/G snv 0.55
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs1344674
rs1344674
3 141406344 intron variant A/G snv 0.55
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2011 2011
dbSNP: rs1344674
rs1344674
3 141406344 intron variant A/G snv 0.55
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
0.700 1.000 1 2017 2017
dbSNP: rs1346408
rs1346408
3 141353447 intron variant C/T snv 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1346408
rs1346408
3 141353447 intron variant C/T snv 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs1582874
rs1582874
3 141396377 5 prime UTR variant T/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1582874
rs1582874
3 141396377 5 prime UTR variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs16851397
rs16851397
3 141415976 intron variant A/G snv 6.3E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs16851397
rs16851397
3 141415976 intron variant A/G snv 6.3E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs1991431
rs1991431
3 141414608 intron variant G/A snv 0.50
Prostate specific antigen measurement
0.700 1.000 1 2017 2017
dbSNP: rs1991431
rs1991431
3 141414608 intron variant G/A snv 0.50
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2013 2013
dbSNP: rs1991431
rs1991431
3 141414608 intron variant G/A snv 0.50
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012