Source: GWASCAT

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: rs3760776
rs3760776
FUT6
0.925 0.120 19 5839735 upstream gene variant G/A snv 0.22
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.800 1.000 1 2012 2012
dbSNP: rs708686
rs708686
FUT6
19 5840608 upstream gene variant C/T snv 0.46
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 2 2018 2018
dbSNP: rs10409772
rs10409772
FUT6
19 5840915 upstream gene variant C/A;G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10420107
rs10420107
FUT6
19 5833268 intron variant G/A snv 0.44
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12019136
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs12019136
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		0.700 1.000 1 2016 2016
dbSNP: rs12019136
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12
CUI: C0271084
Disease: Exudative age-related macular degeneration
Exudative age-related macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs12019136
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs3760775
rs3760775
FUT6
19 5841345 upstream gene variant G/T snv 0.15
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.700 1.000 1 2017 2017
dbSNP: rs3760775
rs3760775
FUT6
19 5841345 upstream gene variant G/T snv 0.15
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs708686
rs708686
FUT6
19 5840608 upstream gene variant C/T snv 0.46
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		0.700 1.000 1 2018 2018
dbSNP: rs708686
rs708686
FUT6
19 5840608 upstream gene variant C/T snv 0.46
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.700 1.000 1 2017 2017
dbSNP: rs778798
rs778798
FUT6
19 5839602 5 prime UTR variant A/C snv 0.82
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs778809
rs778809
FUT6
19 5830291 downstream gene variant G/A;T snv 0.44
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018