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: rs9913911
rs9913911
GAS7
4 0.925 0.040 17 10127866 intron variant A/G snv 0.32 0.700 1.000 6 2014 2018
dbSNP: rs10918274
rs10918274
TMCO1
2 1.000 0.040 1 165745179 intron variant T/C snv 0.89 0.700 1.000 3 2017 2018
dbSNP: rs11217878
rs11217878
ARHGEF12
2 1.000 0.040 11 120469674 intron variant G/A snv 0.20 0.700 1.000 3 2015 2018
dbSNP: rs113542380
rs113542380
THADA
5 2 43237679 intron variant G/A snv 4.7E-02 0.700 1.000 3 2018 2018
dbSNP: rs113985657
rs113985657
EXOC2
2 1.000 0.040 6 597203 intron variant C/T snv 0.14 0.700 1.000 3 2018 2018
dbSNP: rs1579050
rs1579050
FMNL2
3 0.925 0.040 2 152508013 intron variant A/G snv 0.42 0.700 1.000 3 2018 2018
dbSNP: rs163524
rs163524
LINC01833
1 2 44930414 intron variant C/A snv 0.20 0.700 1.000 3 2018 2018
dbSNP: rs3743860
rs3743860
FANCA
1 16 89752083 intron variant T/C snv 0.47 0.700 1.000 3 2018 2018
dbSNP: rs4141194
rs4141194
PLEKHA7
1 11 16989629 intron variant C/A snv 0.20 0.700 1.000 3 2018 2018
dbSNP: rs4775427
rs4775427
LOC107984782
1 15 61659036 intron variant C/T snv 0.42 0.700 1.000 3 2018 2018
dbSNP: rs6732795
rs6732795
ANTXR1
1 2 69184385 intron variant A/C snv 0.51 0.700 1.000 3 2017 2018
dbSNP: rs7555523
rs7555523
TMCO1
4 0.925 0.040 1 165749742 intron variant C/A snv 0.88 0.700 1.000 3 2012 2017
dbSNP: rs7635832
rs7635832
FNDC3B
1 3 172271486 intron variant T/G snv 0.22 0.700 1.000 3 2017 2018
dbSNP: rs7924522
rs7924522
ETS1
2 1.000 0.040 11 128510847 intron variant C/A snv 0.70 0.700 1.000 3 2018 2018
dbSNP: rs9494457
rs9494457
PDE7B
2 1.000 0.040 6 136153656 intron variant T/A snv 0.39 0.700 1.000 3 2018 2018
dbSNP: rs9608740
rs9608740
EMID1 ; LOC105372985
3 22 29224336 intron variant A/C;G;T snv 0.700 1.000 3 2018 2018
dbSNP: rs10189434
rs10189434
BABAM2
1 2 28135884 intron variant C/T snv 0.23 0.700 1.000 2 2018 2018
dbSNP: rs10852918
rs10852918
GAS7
1 17 9937184 intron variant A/G snv 0.49 0.700 1.000 2 2018 2018
dbSNP: rs10869665
rs10869665
PCSK5
1 9 75904083 intron variant C/T snv 0.31 0.700 1.000 2 2018 2018
dbSNP: rs11217863
rs11217863
ARHGEF12
2 11 120422429 intron variant G/A snv 8.6E-02 0.700 1.000 2 2015 2018
dbSNP: rs11616662
rs11616662 		2 13 40545329 intron variant G/A snv 0.11 0.700 1.000 2 2017 2018
dbSNP: rs11656696
rs11656696
GAS7
5 0.882 0.040 17 10130362 intron variant C/A snv 0.36 0.700 1.000 2 2012 2017
dbSNP: rs11659764
rs11659764
LOC105372130
2 18 55668281 intron variant T/A snv 3.2E-02 0.700 1.000 2 2017 2018
dbSNP: rs11795066
rs11795066
RALGPS1 ; ANGPTL2
1 9 127100889 intron variant G/A snv 0.31 0.700 1.000 2 2018 2018
dbSNP: rs12377624
rs12377624
LOC105376277
2 1.000 0.040 9 126610831 intron variant G/C snv 0.28 0.700 1.000 2 2018 2018