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: rs16917667
rs16917667
C8orf37-AS1
1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 2 2018 2019
dbSNP: rs10113800
rs10113800
C8orf37-AS1
1.000 0.040 8 95432774 non coding transcript exon variant G/A snv 0.31
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs16917667
rs16917667
C8orf37-AS1
1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2019 2019
dbSNP: rs16917667
rs16917667
C8orf37-AS1
1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02
CUI: C4022792
Disease: Reduced ejection fraction
Reduced ejection fraction 		0.700 1.000 1 2019 2019
dbSNP: rs1873745
rs1873745
C8orf37-AS1
1.000 0.040 8 95434771 intron variant A/G snv 0.24
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs55821258
rs55821258
C8orf37-AS1
8 95279813 intron variant C/G snv 0.11
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs55821258
rs55821258
C8orf37-AS1
8 95279813 intron variant C/G snv 0.11
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs6471530
rs6471530
C8orf37-AS1
1.000 0.040 8 95434448 intron variant G/A;C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs74864598
rs74864598
C8orf37-AS1
1.000 0.040 8 95439207 intron variant C/A snv 4.4E-02
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2019 2019
dbSNP: rs74864598
rs74864598
C8orf37-AS1
1.000 0.040 8 95439207 intron variant C/A snv 4.4E-02
CUI: C4022792
Disease: Reduced ejection fraction
Reduced ejection fraction 		0.700 1.000 1 2019 2019
dbSNP: rs74864598
rs74864598
C8orf37-AS1
1.000 0.040 8 95439207 intron variant C/A snv 4.4E-02
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2019 2019
dbSNP: rs7825742
rs7825742
C8orf37-AS1
8 95404957 intron variant T/C snv 0.17
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019