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: rs10108704
rs10108704 		2 1.000 0.080 8 109350232 downstream gene variant G/T snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs16872704
rs16872704 		2 1.000 0.080 6 12345461 intergenic variant A/G snv 0.22 0.700 1.000 1 2016 2016
dbSNP: rs4900006
rs4900006
LOC105370616 ; LOC105370617
2 1.000 0.080 14 89642343 intron variant C/A snv 5.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs7715147
rs7715147
ELOVL7
2 1.000 0.080 5 60757393 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs78523330
rs78523330
FBXO47
2 1.000 0.080 17 38949729 intron variant A/G snv 2.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
5 0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 0.700 1.000 1 2016 2016