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: rs2920297
rs2920297
PSCA ; JRK
1 1.000 0.040 8 142681665 3 prime UTR variant A/G snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs2976392
rs2976392
PSCA ; JRK
15 0.724 0.240 8 142681514 3 prime UTR variant G/A snv 0.46 0.45 0.010 1.000 1 2019 2019
dbSNP: rs2294008
rs2294008
PSCA ; JRK
28 0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 0.860 1.000 6 2012 2019
dbSNP: rs2164308
rs2164308
LY6K ; LNCOC1
1 1.000 0.040 8 142704241 3 prime UTR variant C/T snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs2572904
rs2572904
LNCOC1
1 1.000 0.040 8 142710775 intron variant A/C snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs2585140
rs2585140
THEM6 ; LNCOC1
1 1.000 0.040 8 142725478 intron variant A/G snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs10434
rs10434
VEGFA
17 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 0.010 1.000 1 2009 2009
dbSNP: rs28473387
rs28473387 		1 1.000 0.040 8 142626112 intergenic variant T/C snv 0.63 0.700 1.000 1 2012 2012