Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10212439
rs10212439
LOC100507389
1 3 142936211 non coding transcript exon variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs174560
rs174560
FADS1 ; FADS2
5 1.000 0.080 11 61814292 non coding transcript exon variant T/C snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs174594
rs174594
FADS2
14 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs28456
rs28456
FADS1 ; FADS2
5 0.925 0.120 11 61822009 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4520
rs4520
APOC3
1 11 116830819 synonymous variant T/C snv 0.65 0.70 0.700 1.000 1 2019 2019
dbSNP: rs8736
rs8736
MBOAT7 ; TMC4 ; LOC112268246
1 19 54173495 3 prime UTR variant T/C snv 0.61 0.700 1.000 1 2019 2019