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: rs1537370
rs1537370
CDKN2B-AS1
2 1.000 9 22084311 intron variant C/T snv 0.55 0.800 1.000 3 2011 2013
dbSNP: rs10511701
rs10511701
CDKN2B-AS1
2 9 22112600 intron variant T/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs1333043
rs1333043
CDKN2B-AS1
2 9 22106732 intron variant T/A snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs1537371
rs1537371
CDKN2B-AS1
1 9 22099569 intron variant C/A;T snv 0.700 1.000 2 2011 2013
dbSNP: rs1556516
rs1556516
CDKN2B-AS1
1 9 22100177 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs7341786
rs7341786
CDKN2B-AS1
2 9 22112242 intron variant A/C snv 0.65 0.700 1.000 2 2011 2013
dbSNP: rs10127775
rs10127775
GALNT2
4 1 230160042 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10211524
rs10211524
LINC02245 ; LOC107984063
4 2 64980940 intron variant G/A snv 0.51 0.700 1.000 1 2012 2012
dbSNP: rs10500569
rs10500569
LOC107984814
1 16 72722202 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10502575
rs10502575 		1 18 31756628 downstream gene variant A/G snv 6.9E-02 0.800 1.000 1 2013 2013
dbSNP: rs10807323
rs10807323
PHACTR1
1 6 12794799 intron variant G/A snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs12051548
rs12051548
TM4SF5
1 17 4779740 intron variant G/C snv 7.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs12507628
rs12507628 		1 4 72779634 regulatory region variant G/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs1333050
rs1333050
CDKN2B-AS1
1 9 22125914 intron variant C/T snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs16850360
rs16850360 		2 4 74006728 intron variant A/G snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs16939881
rs16939881
AQP9 ; ALDH1A2
2 15 58179780 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17404667
rs17404667
PRICKLE2
1 3 64288876 intron variant C/G snv 6.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs1851024
rs1851024 		1 4 71842104 intergenic variant G/A snv 0.93 0.700 1.000 1 2012 2012
dbSNP: rs188234402
rs188234402
CDKN2B-AS1
1 9 22029058 intron variant T/A snv 2.1E-05 0.700 1.000 1 2013 2013
dbSNP: rs1912826
rs1912826
KLKB1
4 4 186228386 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1998013
rs1998013 		1 1 55492357 intron variant C/T snv 4.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs201049435
rs201049435
CDKN2B-AS1
1 9 22029059 intron variant AA/-;A;AAA;AAAA delins 6.9E-03 0.700 1.000 1 2013 2013
dbSNP: rs2168889
rs2168889 		1 4 74357994 intergenic variant A/G snv 4.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs217181
rs217181
TXNL4B
6 16 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs2306786
rs2306786
MYO1E
1 15 59195731 intron variant C/G snv 8.0E-02 0.700 1.000 1 2012 2012