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: rs10739221
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs10739221
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv
CUI: C0153535
Disease: Malignant melanoma of skin of upper limb
Malignant melanoma of skin of upper limb 		0.700 1.000 1 2015 2015
dbSNP: rs10739221
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv
CUI: C0153536
Disease: Malignant melanoma of skin of lower limb
Malignant melanoma of skin of lower limb 		0.700 1.000 1 2015 2015
dbSNP: rs10739221
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2017 2017
dbSNP: rs10739221
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.700 1.000 1 2015 2015