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: rs1008924
rs1008924
FRMD6
1 14 51616362 intron variant G/A snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10235512
rs10235512
RADIL
1 7 4865424 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10255299
rs10255299
DOCK4
2 7 111887504 intron variant G/A snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs10429953
rs10429953
CR1
1 1 207615233 intron variant A/G snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs10435719
rs10435719 		2 8 11919395 downstream gene variant C/T snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs10437339
rs10437339 		1 1 159740595 intergenic variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10437340
rs10437340 		1 1 159741019 intergenic variant G/C snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs10485165
rs10485165
LOC105377885
3 6 88403098 intron variant C/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs10512597
rs10512597
CD300LF ; RAB37
4 17 74703694 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10744775
rs10744775
BRAP
2 12 111658411 intron variant T/C snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs10751037
rs10751037 		1 11 81025386 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10761731
rs10761731
JMJD1C
6 10 63267850 intron variant A/T snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs10774580
rs10774580
OASL
1 12 121038620 intron variant A/G snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs10778213
rs10778213
C12orf42
1 12 103101373 intron variant T/C snv 0.57 0.800 1.000 1 2008 2008
dbSNP: rs10778215
rs10778215
C12orf42
2 12 103143488 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
5 15 58431280 intron variant T/C snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs10779330
rs10779330
CR1
1 1 207589329 intron variant G/A snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs10789192
rs10789192 		1 1 65660087 intergenic variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs10838687
rs10838687
MADD
2 11 47291341 intron variant T/G snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs10863358
rs10863358
CR1
1 1 207517526 intron variant G/C snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs10888935
rs10888935 		1 1 55595278 intron variant T/A snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs10891343
rs10891343
BCO2
2 11 112209661 intron variant T/C snv 0.44 0.700 1.000 1 2014 2014
dbSNP: rs10908713
rs10908713 		2 1 159369769 intron variant T/C snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10908716
rs10908716
OR10J1
1 1 159406553 intron variant A/G snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs10908717
rs10908717
OR10J1
1 1 159406562 intron variant C/A snv 0.10 0.700 1.000 1 2012 2012