Source: GWASDB

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: rs10503899
rs10503899
NRG1 ; NRG1-IT1
1.000 0.040 8 32089718 intron variant A/G snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2012 2012
dbSNP: rs10954843
rs10954843
NRG1
8 32419595 intron variant G/A snv 0.97
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10954843
rs10954843
NRG1
8 32419595 intron variant G/A snv 0.97
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16879344
rs16879344
NRG1
8 32405005 intron variant G/A snv 5.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2347510
rs2347510
NRG1
8 32384283 intron variant G/A snv 0.90
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4512342
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2007 2007