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: rs2524299
rs2524299
FADS2
2 11 61837310 intron variant A/T snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs2526678
rs2526678
FADS2
2 11 61856321 non coding transcript exon variant G/A snv 8.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs2727270
rs2727270
FADS2
2 11 61835765 intron variant C/T snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs2727271
rs2727271
FADS2
2 11 61835886 intron variant A/T snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs2845573
rs2845573
FADS2
3 1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs2851682
rs2851682
FADS2
5 11 61848540 intron variant A/G snv 9.9E-02 0.700 1.000 1 2011 2011
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: 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: 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: rs695867
rs695867
TMEM258 ; FEN1 ; FADS2 ; MIR611
1 11 61793816 intron variant A/G snv 2.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs7935946
rs7935946
FADS2
2 11 61848070 5 prime UTR variant C/T snv 0.11 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
dbSNP: rs968567
rs968567
FADS1 ; FADS2
7 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011