Gene: FADS2 ×
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: rs4246215
rs4246215
FEN1 ; FADS2
29 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs526126
rs526126
FADS2
3 1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 0.700 1.000 1 2011 2011
dbSNP: rs174605
rs174605
FADS2
2 11 61859449 intron variant G/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs174591
rs174591
FADS2
2 11 61850204 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs174541
rs174541
FADS2
8 1.000 0.080 11 61798436 intron variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs174547
rs174547
FADS1 ; FADS2
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs174550
rs174550
FADS1 ; FADS2
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs174593
rs174593
FADS2
2 11 61851359 intron variant T/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs174602
rs174602
FADS2
3 1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs174611
rs174611
FADS2
2 11 61860409 intron variant T/C snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs17831757
rs17831757
FADS2
2 11 61867728 downstream gene variant T/C snv 9.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs498793
rs498793
FADS2
3 1.000 0.040 11 61857233 intron variant T/C snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs916924
rs916924
FADS2
2 11 61851709 intron variant T/C snv 9.1E-02 0.700 1.000 1 2011 2011