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: rs13412535
rs13412535
SERPINE2
5 2 224010157 intron variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs1545747
rs1545747
MEGF11
3 15 66164979 intron variant G/T snv 0.97 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
dbSNP: rs7615304
rs7615304
LEKR1
1 3 156957914 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs77670845
rs77670845
CPED1
1 7 121229508 intron variant ATGAA/- delins 0.45 0.700 1.000 1 2017 2017
dbSNP: rs79992897
rs79992897 		1 2 223326960 intergenic variant G/C snv 7.5E-04 0.700 1.000 1 2017 2017