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: rs72700114
rs72700114
LINC01681
1.000 0.080 1 170224684 intron variant G/C snv 7.3E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 3 2018 2018
dbSNP: rs72700118
rs72700118
LINC01681
1.000 0.080 1 170225682 intron variant C/A;T snv 7.9E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 2 2017 2018
dbSNP: rs10800507
rs10800507
LINC01681
1.000 0.080 1 170216500 intron variant C/G snv 0.47
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2017 2017
dbSNP: rs113976843
rs113976843
LINC01681
1 170254627 intron variant T/C snv 8.6E-03
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2019 2019
dbSNP: rs12122060
rs12122060
LINC01681
1.000 0.080 1 170224718 intron variant T/A snv 7.9E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs4656744
rs4656744
LINC01681
1 170200953 intron variant T/A snv 0.33
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs71635652
rs71635652
LINC01681
1.000 0.080 1 170255221 intron variant T/G snv 0.21
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017