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: rs9581943
rs9581943
PDX1
1 1.000 0.120 13 27919860 upstream gene variant G/A snv 0.31 0.700 1.000 3 2014 2018
dbSNP: rs1486134
rs1486134 		1 1.000 0.120 2 67412637 downstream gene variant G/C;T snv 0.700 1.000 2 2015 2018
dbSNP: rs1517037
rs1517037 		3 0.882 0.120 18 59211042 intergenic variant C/T snv 0.23 0.710 0.500 2 2015 2018
dbSNP: rs16986825
rs16986825
ZNRF3
1 1.000 0.120 22 28904318 intron variant C/T snv 0.13 0.700 1.000 2 2014 2018
dbSNP: rs17688601
rs17688601
SUGCT ; LOC112267984
1 1.000 0.120 7 40827064 intron variant C/A snv 0.20 0.700 1.000 2 2015 2018
dbSNP: rs2816938
rs2816938 		2 1.000 0.120 1 200016240 upstream gene variant T/A snv 0.37 0.700 1.000 2 2016 2018
dbSNP: rs2900174
rs2900174
PRB1 ; PRB2
1 1.000 0.120 12 11394598 intron variant A/G snv 0.12 0.800 1.000 2 2012 2017
dbSNP: rs35226131
rs35226131
TERT
2 1.000 0.120 5 1295258 upstream gene variant C/T snv 2.6E-02 0.700 1.000 2 2016 2018
dbSNP: rs6971499
rs6971499
LINC-PINT
1 1.000 0.120 7 130995762 intron variant T/C snv 0.15 0.700 1.000 2 2014 2018
dbSNP: rs7190458
rs7190458
BCAR1
1 1.000 0.120 16 75229763 synonymous variant G/A snv 5.1E-02 0.11 0.700 1.000 2 2014 2018
dbSNP: rs1034925236
rs1034925236
NR5A2
2 0.925 0.120 1 200048258 missense variant G/C snv 0.010 1.000 1 2011 2011
dbSNP: rs1049074086
rs1049074086
CTSD
9 0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs10500715
rs10500715
SBF2
2 0.925 0.120 11 9951515 intron variant T/G snv 0.39 0.700 1.000 1 2014 2014
dbSNP: rs10835188
rs10835188
LIN7C
2 1.000 0.120 11 27501639 intron variant G/T snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs10887710
rs10887710 		2 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs10983614
rs10983614
ASTN2
1 1.000 0.120 9 117306874 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs11085754
rs11085754
SMARCA4
2 0.925 0.120 19 11017920 intron variant A/G snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs111033565
rs111033565
PRSS1
11 0.742 0.120 7 142751938 missense variant G/A snv 1.2E-05 0.010 1.000 1 2008 2008
dbSNP: rs1131691021
rs1131691021
TP53
21 0.716 0.120 17 7675097 missense variant A/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs11644043
rs11644043
BRD7
2 0.925 0.120 16 50327466 intron variant T/C snv 0.24 0.010 1.000 1 2015 2015
dbSNP: rs11644322
rs11644322
WWOX
3 0.925 0.120 16 79005703 intron variant C/T snv 0.22 0.010 1.000 1 2016 2016
dbSNP: rs1169296
rs1169296
HNF1A
1 1.000 0.120 12 120990604 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs1176026649
rs1176026649
PALLD ; CBR4
4 0.851 0.120 4 168921582 missense variant C/T snv 7.2E-06 0.010 1.000 1 2007 2007
dbSNP: rs1182933
rs1182933
C12orf43
3 1.000 0.120 12 121016819 upstream gene variant C/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs12029406
rs12029406 		3 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 0.010 1.000 1 2018 2018