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: rs712964
rs712964 		2 22 19168604 upstream gene variant T/C snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs8134546
rs8134546
LINC01426
2 1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs4810479
rs4810479 		7 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs445925
rs445925
APOC1
10 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs6511720
rs6511720
LDLR
15 0.790 0.120 19 11091630 intron variant G/T snv 0.12 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: rs616082
rs616082 		1 18 31787677 intergenic variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs6506897
rs6506897 		2 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 0.700 1.000 1 2017 2017
dbSNP: rs6506900
rs6506900
LOC105372049
2 1.000 0.080 18 31226433 intergenic variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs8089491
rs8089491 		1 18 31763291 upstream gene variant G/A snv 5.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs115689251
rs115689251
LOC107985068
2 1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs12051548
rs12051548
TM4SF5
1 17 4779740 intron variant G/C snv 7.5E-02 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: rs173539
rs173539 		11 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 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: rs4788815
rs4788815
LOC105371334
3 16 71600908 intergenic variant A/T snv 0.69 0.700 1.000 1 2012 2012
dbSNP: rs1532085
rs1532085
ALDH1A2
13 0.882 0.080 15 58391167 intron variant A/G;T snv 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: rs2306786
rs2306786
MYO1E
1 15 59195731 intron variant C/G snv 8.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs6606859
rs6606859
GABRG3
2 1.000 0.080 15 27032254 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs77757620
rs77757620
STARD9
2 1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs1303
rs1303
SERPINA1
4 0.925 0.040 14 94378506 missense variant T/G snv 0.28 0.22 0.700 1.000 1 2012 2012
dbSNP: rs3809346
rs3809346
COL4A1 ; COL4A2
2 1.000 0.080 13 110308596 intron variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs448792
rs448792
FRY
2 1.000 0.080 13 32103287 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs543554
rs543554
FRY
2 1.000 0.080 13 32127501 intron variant A/G;T snv 0.700 1.000 1 2017 2017