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: rs724577
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2013
dbSNP: rs6830062
rs6830062
LCORL
4 18016107 intron variant T/C snv 0.25
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2008 2019
dbSNP: rs13131350
rs13131350
LCORL
4 17875864 synonymous variant A/G snv 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2015 2019
dbSNP: rs16896068
rs16896068
LCORL
4 17943217 intron variant G/A snv 0.25
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2008 2019
dbSNP: rs2724475
rs2724475
LCORL
4 17944809 intron variant T/C snv 0.71
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs6830062
rs6830062
LCORL
4 18016107 intron variant T/C snv 0.25
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2009
dbSNP: rs724577
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2011 2019
dbSNP: rs7692995
rs7692995
LCORL
4 17935011 intron variant T/C snv 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs925098
rs925098
LCORL
4 17918188 intron variant G/A snv 0.70
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2012 2019
dbSNP: rs925098
rs925098
LCORL
4 17918188 intron variant G/A snv 0.70
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2011 2012
dbSNP: rs114192810
rs114192810
LCORL
4 17967519 intron variant T/G snv 1.5E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1380294
rs1380294
LCORL
4 18022498 upstream gene variant C/T snv 0.25
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs1380294
rs1380294
LCORL
4 18022498 upstream gene variant C/T snv 0.25
CUI: C0455806
Disease: Infant length
Infant length 		0.700 1.000 1 2015 2015
dbSNP: rs16896068
rs16896068
LCORL
4 17943217 intron variant G/A snv 0.25
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008
dbSNP: rs16896210
rs16896210
LCORL
4 17990709 intron variant A/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs16896261
rs16896261
LCORL
4 18009579 intron variant A/G snv 0.21
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs185373991
rs185373991
LCORL
1.000 0.080 4 17864241 intron variant T/A snv 9.1E-02
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2018 2018
dbSNP: rs2011603
rs2011603
LCORL
4 18023861 upstream gene variant G/A snv 0.70
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2012 2012
dbSNP: rs2061456
rs2061456
LCORL
4 17996803 intron variant C/A snv 0.21
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs2174633
rs2174633
LCORL
4 17916158 intron variant A/C snv 0.70
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs2320299
rs2320299
LCORL
4 17970749 intron variant G/A snv 0.69
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs2610990
rs2610990
LCORL
4 18006609 intron variant A/G snv 0.73
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2707450
rs2707450
LCORL
4 17940937 intron variant C/T snv 0.73
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2707450
rs2707450
LCORL
4 17940937 intron variant C/T snv 0.73
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
dbSNP: rs2707450
rs2707450
LCORL
4 17940937 intron variant C/T snv 0.73
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019