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: rs1009358
rs1009358
LINC02245 ; LINC02576 ; LOC107984063
2 1.000 0.080 2 65049318 intron variant T/C snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10107066
rs10107066
DPYSL2
1 8 26542619 intron variant G/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10116277
rs10116277
CDKN2B-AS1
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.010 < 0.001 1 2013 2013
dbSNP: rs10224002
rs10224002
PRKAG2
12 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs10224210
rs10224210
PRKAG2
9 1.000 0.040 7 151716108 intron variant T/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1030431
rs1030431 		3 8 58399138 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10306135
rs10306135
PTGS1
1 9 122375416 5 prime UTR variant A/T snv 0.14 0.010 1.000 1 2009 2009
dbSNP: rs10409243
rs10409243
DNMT1 ; S1PR2
6 19 10222312 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1042309696
rs1042309696
ACE
2 17 63487006 synonymous variant T/C snv 0.010 1.000 1 2008 2008
dbSNP: rs1042580
rs1042580
THBD
2 20 23046984 3 prime UTR variant T/C snv 0.33 0.010 1.000 1 2007 2007
dbSNP: rs1044486
rs1044486
USP36
1 17 78796097 3 prime UTR variant G/A snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs1047964
rs1047964
BACE1 ; RNF214
3 11 117286177 3 prime UTR variant G/A;C;T snv 0.710 1.000 1 2011 2011
dbSNP: rs1048070
rs1048070
FREM1
1 9 14735055 3 prime UTR variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10500326
rs10500326
UBN1
1 16 4868325 intron variant G/T snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1058322
rs1058322
ADIPOR2
2 1.000 0.040 12 1727813 intron variant C/T snv 0.30 0.010 1.000 1 2011 2011
dbSNP: rs10740995
rs10740995
CACNB2
1 10 18156159 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1074703
rs1074703
NCALD
1 8 101803258 intron variant C/A snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs10748798
rs10748798
PAX2
1 10 100794914 intron variant C/T snv 0.91 0.700 1.000 1 2019 2019
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
dbSNP: rs10759931
rs10759931 		9 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10769254
rs10769254
MYBPC3
4 11 47340914 intron variant G/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10816914
rs10816914
PALM2AKAP2
1 9 109998608 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10821967
rs10821967
RTKN2
1 10 62182180 downstream gene variant A/G snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs10824134
rs10824134
ADK
1 10 74261866 intron variant T/C snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs10832571
rs10832571
SOX6
1 11 16239678 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019