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: rs174528
rs174528
MYRF ; TMEM258
5 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 1 2015 2015
dbSNP: rs174545
rs174545
FADS1 ; FADS2
5 1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs174577
rs174577
FADS2
13 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs2581624
rs2581624 		2 3 142915027 intron variant G/C;T snv 0.29 0.700 1.000 1 2015 2015