Source: ALL

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: rs845084
rs845084
LINC02641
1.000 0.040 10 123460520 intron variant G/A snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs11248566
rs11248566
LINC02641
1.000 0.040 10 123515942 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11597044
rs11597044
LINC02641
1.000 0.040 10 123460740 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1219960
rs1219960
LINC02641
1.000 0.040 10 123458091 intron variant T/C snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1568079
rs1568079
LINC02641
10 123492235 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs2282015
rs2282015
LINC02641
1.000 0.040 10 123462521 intron variant T/G snv 0.39
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2282015
rs2282015
LINC02641
1.000 0.040 10 123462521 intron variant T/G snv 0.39
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2013 2013
dbSNP: rs4980297
rs4980297
LINC02641
1.000 0.040 10 123515847 intron variant T/C snv 0.33
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6599698
rs6599698
LINC02641
1.000 0.040 10 123462759 intron variant C/T snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs705145
rs705145
LINC02641
1.000 0.040 10 123466662 intron variant C/A;T snv
CUI: C0026603
Disease: Motion Sickness
Motion Sickness 		0.700 1.000 1 2015 2015
dbSNP: rs7090367
rs7090367
LINC02641
10 123474976 intron variant T/C snv 0.38
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs7091877
rs7091877
LINC02641
1.000 0.040 10 123459725 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs845083
rs845083
LINC02641
1.000 0.040 10 123462218 intron variant T/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs845084
rs845084
LINC02641
1.000 0.040 10 123460520 intron variant G/A snv 0.26
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017