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: rs144701438
rs144701438 		1 18 66293168 intergenic variant G/A snv 2.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs147747784
rs147747784 		2 19 54606728 upstream gene variant G/C snv 2.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs182429465
rs182429465
PAQR8 ; EFHC1
1 6 52390889 intron variant T/C snv 3.3E-03 0.700 1.000 1 2017 2017
dbSNP: rs4320361
rs4320361 		1 6 43960774 intergenic variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs5893521
rs5893521
LOC105375670
1 8 100462867 intron variant T/-;TT delins 0.46 0.700 1.000 1 2017 2017
dbSNP: rs62006410
rs62006410 		1 14 102541598 upstream gene variant C/T snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs75904417
rs75904417
B3GALT1
1 2 167796811 intergenic variant A/C snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs77981494
rs77981494
XYLT1
1 16 17451009 intron variant T/C snv 3.8E-02 0.700 1.000 1 2017 2017