Source: GWASCAT

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: rs10146997
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.800 1.000 1 2009 2009
dbSNP: rs11624704
rs11624704
NRXN3
1.000 0.080 14 78319734 intron variant A/C snv 0.13
CUI: C0028754
Disease: Obesity
Obesity 		0.800 1.000 1 2011 2011
dbSNP: rs2370983
rs2370983
NRXN3
1.000 0.080 14 79437033 intron variant G/A snv 0.71
CUI: C0028754
Disease: Obesity
Obesity 		0.800 1.000 1 2013 2013
dbSNP: rs7141420
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56
CUI: C0028754
Disease: Obesity
Obesity 		0.800 1.000 1 2013 2013
dbSNP: rs7144011
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.800 1.000 1 2009 2015
dbSNP: rs7141420
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 6 2015 2019
dbSNP: rs10150332
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2010 2019
dbSNP: rs11621908
rs11621908
NRXN3
14 78029418 regulatory region variant C/T snv 0.11
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 2 2019 2019
dbSNP: rs17109256
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2015 2019
dbSNP: rs7144011
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2018 2019
dbSNP: rs10136360
rs10136360
NRXN3
14 79427703 intron variant G/A snv 0.21
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		0.700 1.000 1 2019 2019
dbSNP: rs10146997
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2017 2017
dbSNP: rs11849937
rs11849937
NRXN3
1.000 0.040 14 78645876 intron variant C/T snv 0.11
CUI: C0270496
Disease: Schizoaffective disorder, bipolar type
Schizoaffective disorder, bipolar type 		0.700 1.000 1 2019 2019
dbSNP: rs12882688
rs12882688
NRXN3 ; LOC112268125
14 79247254 splice region variant G/A snv 0.25
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs17109221
rs17109221
NRXN3
14 79443776 intron variant C/T snv 0.21
CUI: C0005910
Disease: Body Weight
Body Weight 		0.700 1.000 1 2017 2017
dbSNP: rs17109256
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2370901
rs2370901
NRXN3
14 79105688 intron variant C/T snv 0.50
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2370982
rs2370982
NRXN3
14 79424334 intron variant C/T snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs7141420
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs7141420
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs7141420
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7144011
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2015 2015
dbSNP: rs7144011
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs72690737
rs72690737
NRXN3
14 79464301 intron variant T/C snv 0.18
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs8009329
rs8009329
NRXN3
14 79029342 intron variant A/G snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019