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: rs112058662
rs112058662 		1 7 149673022 intergenic variant -/AAGA delins 0.27 0.700 1.000 1 2017 2017
dbSNP: rs113600793
rs113600793
EFCAB13
3 17 47384095 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs116609577
rs116609577
PALLD
1 4 168799231 intron variant T/C snv 4.9E-03 0.700 1.000 1 2017 2017
dbSNP: rs143014767
rs143014767
JMJD1C
1 10 63304077 intron variant CTTTGCC/- del 0.700 1.000 1 2017 2017
dbSNP: rs147378920
rs147378920 		1 1 22375502 intergenic variant A/G snv 1.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs187784918
rs187784918 		2 1 22671357 intergenic variant T/A snv 0.700 1.000 1 2017 2017
dbSNP: rs2188420
rs2188420 		1 7 106845798 intergenic variant C/G snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs45498698
rs45498698
EPHA8
3 1 22569327 missense variant G/A snv 6.7E-03 7.1E-03 0.700 1.000 1 2017 2017
dbSNP: rs73479333
rs73479333 		1 6 82269213 upstream gene variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs75885714
rs75885714
PLCL2
7 3 16901018 intron variant A/C snv 4.6E-02 0.700 1.000 1 2018 2018