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: rs16879552
rs16879552
NRG1
0.882 0.080 8 32553698 intron variant C/T snv 0.10
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.850 0.833 1 2009 2019
dbSNP: rs2439302
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.830 1.000 1 2012 2015
dbSNP: rs7825175
rs7825175
NRG1
8 32558756 intron variant G/A snv 0.18
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.800 1.000 1 2013 2013
dbSNP: rs4236709
rs4236709
NRG1
0.925 0.080 8 32552592 intron variant G/A;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 2 2017 2019
dbSNP: rs4489283
rs4489283
NRG1
8 32542144 intron variant T/C snv 0.59
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 2 2019 2019
dbSNP: rs7005606
rs7005606
NRG1
0.925 0.080 8 32543983 intron variant T/G snv 0.39
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
Congenital Intestinal Aganglionosis 		0.700 1.000 2 2014 2016
dbSNP: rs7005606
rs7005606
NRG1
0.925 0.080 8 32543983 intron variant T/G snv 0.39
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 1.000 2 2014 2016
dbSNP: rs10088648
rs10088648
NRG1
1.000 8 32523319 intron variant A/T snv 0.56
CUI: C4021813
Disease: Oral cleft
Oral cleft 		0.700 1.000 1 2017 2017
dbSNP: rs10102889
rs10102889
NRG1
8 32578102 intron variant C/G snv 9.0E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs1481757
rs1481757
NRG1 ; NRG1-IT1
8 32110442 intron variant T/C snv 0.72
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2016 2016
dbSNP: rs16879552
rs16879552
NRG1
0.882 0.080 8 32553698 intron variant C/T snv 0.10
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
Congenital Intestinal Aganglionosis 		0.700 1.000 1 2009 2009
dbSNP: rs17673138
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2015 2015
dbSNP: rs17673138
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs17673138
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.700 1.000 1 2015 2015
dbSNP: rs17673138
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2015 2015
dbSNP: rs1878918
rs1878918
NRG1
0.925 0.120 8 32476054 intron variant G/A;C snv
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.700 1.000 1 2017 2017
dbSNP: rs1878918
rs1878918
NRG1
0.925 0.120 8 32476054 intron variant G/A;C snv
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.700 1.000 1 2017 2017
dbSNP: rs200393053
rs200393053
NRG1
8 32736709 intron variant T/-;TT delins
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs2466075
rs2466075
NRG1
1.000 0.040 8 32575431 intron variant A/G snv 0.51
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2016 2016
dbSNP: rs2466076
rs2466076
NRG1
1.000 0.080 8 32575278 intron variant G/T snv 0.53
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs2466077
rs2466077
NRG1
8 32575235 intron variant G/T snv 0.53
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs2466103
rs2466103
NRG1
8 32554786 intron variant T/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs35033136
rs35033136
NRG1
8 32744536 intron variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs4236709
rs4236709
NRG1
0.925 0.080 8 32552592 intron variant G/A;T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs527953512
rs527953512
NRG1
8 32533038 intron variant A/-;AA;AAA;AAAA;AAAAAA delins
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019