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: rs10128898
rs10128898 		12 1385266 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12298813
rs12298813 		12 1349719 intron variant G/C snv 0.54
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs12301937
rs12301937 		1.000 0.040 12 1390472 intron variant A/G snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12321803
rs12321803 		1.000 0.040 12 1390248 intron variant C/T snv 0.29
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6489283
rs6489283 		1.000 0.040 12 1384393 intron variant T/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs766095
rs766095 		1.000 0.040 12 1389267 intron variant G/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7968583
rs7968583 		1.000 0.040 12 1400455 intron variant G/A;C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7971674
rs7971674 		12 1404360 intron variant A/T snv 0.28
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2018 2018
dbSNP: rs7978540
rs7978540 		1.000 0.040 12 1397926 intron variant T/C snv 0.52
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs61740169
rs61740169 		1.000 0.080 12 1027951 missense variant G/C snv 1.5E-03 5.8E-04
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2017 2017