Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10002082
rs10002082 		4 164159753 intron variant A/G snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs10517800
rs10517800 		4 164174438 intron variant C/A;T snv
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs1120384
rs1120384 		4 164161744 intron variant G/A snv 0.16
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs11930019
rs11930019 		4 164159224 intron variant T/C snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs11931264
rs11931264 		4 164160251 intron variant T/C snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs11943491
rs11943491 		4 164159378 intron variant G/A snv 0.18
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs13435288
rs13435288 		4 164169729 intron variant A/G snv 0.19
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs1430998
rs1430998 		4 164164966 intron variant A/G snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs1430999
rs1430999 		4 164164750 intron variant G/A snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs1431001
rs1431001 		4 164164637 intron variant A/T snv 0.18
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs17044565
rs17044565 		4 164148585 intron variant T/C snv 0.19
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs17044630
rs17044630 		4 164157441 intron variant T/A snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs17044711
rs17044711 		4 164172004 intron variant C/T snv 0.12
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs17044858
rs17044858 		4 164280257 intron variant G/A snv 4.8E-02
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.700 1.000 1 2010 2010
dbSNP: rs1835507
rs1835507 		4 164190521 intron variant A/G snv 0.15
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs41445146
rs41445146 		0.925 0.040 4 163810480 intron variant A/G snv 4.9E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs41445146
rs41445146 		0.925 0.040 4 163810480 intron variant A/G snv 4.9E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs6822628
rs6822628 		4 164148204 intron variant G/A snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs6835078
rs6835078 		4 164155752 intron variant C/T snv 0.19
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs6840738
rs6840738 		4 164156275 intron variant A/C snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs723730
rs723730 		4 164154356 intron variant A/T snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs7659131
rs7659131 		4 164180839 intron variant G/A;T snv
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs7673540
rs7673540 		4 164177450 intron variant G/A snv 0.16
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs985676
rs985676 		4 164156960 intron variant T/C snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018
dbSNP: rs9991538
rs9991538 		4 164159680 intron variant T/G snv 0.20
CUI: C0018810
Disease: heart rate
heart rate 		0.700 1.000 1 2018 2018