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: rs587777649
rs587777649
STAT3
1 1.000 17 42322445 missense variant G/A;C snv 4.0E-06 0.800 1.000 2 2014 2017
dbSNP: rs587777650
rs587777650
STAT3
1 1.000 17 42322409 missense variant C/G snv 0.800 1.000 2 2014 2017
dbSNP: rs10202630
rs10202630 		4 0.882 2 190398199 intergenic variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs10444776
rs10444776
LOC112268138
4 0.882 14 105647030 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10494079
rs10494079
VAV3
4 0.882 1 107832253 intron variant G/C snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs10937560
rs10937560
MB21D2
4 0.882 3 192909627 intron variant G/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10986284
rs10986284 		4 0.882 9 124236874 intergenic variant A/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs11086102
rs11086102 		6 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs11746555
rs11746555
SLC22A5
4 0.882 5 132391341 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11785816
rs11785816
LINC00824
4 0.882 8 128518940 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1199047
rs1199047
CCDC88B
4 0.882 11 64350711 intron variant A/C snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs12980063
rs12980063
CPT1C
4 0.882 19 49693735 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs1320344
rs1320344
C12orf42
4 0.882 12 103493699 intron variant A/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs13299616
rs13299616
PSMD5 ; CUTALP
4 0.882 9 120832525 intron variant T/C snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs13380830
rs13380830
RAB5C
4 0.882 17 42145640 intron variant C/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs142647938
rs142647938
KCNH7
4 0.882 2 162516642 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs145268310
rs145268310 		4 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs1530687
rs1530687
ARHGAP31
4 0.882 3 119395668 intron variant G/A snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs1549922
rs1549922 		4 0.882 5 159304540 intergenic variant G/A snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs1790588
rs1790588
CD226
4 0.882 18 69867948 intron variant T/C snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs1800601
rs1800601
NTRK1 ; SH2D2A
4 0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs191252491
rs191252491
ALDH2
4 0.882 12 111773070 intron variant A/T snv 7.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1921445
rs1921445 		4 0.882 3 106229671 intergenic variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs2075302
rs2075302
FAP
5 0.882 2 162219636 intron variant T/C snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs2093816
rs2093816
LINC02341
4 0.882 13 42471900 intron variant C/T snv 0.47 0.700 1.000 1 2019 2019