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: rs10021465
rs10021465
FAM13A
4 4 88829210 intron variant A/G snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs1040526
rs1040526
ADGRG6
2 6 142414679 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs10516527
rs10516527
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105813189 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11134779
rs11134779
ADAM19
2 5 157509758 intron variant A/G snv 0.42 0.700 1.000 1 2010 2010
dbSNP: rs11726124
rs11726124
INTS12 ; GSTCD
2 4 105845339 intron variant A/G snv 5.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11726569
rs11726569
ARHGEF38 ; INTS12
2 4 105685451 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11727735
rs11727735
INTS12 ; GSTCD
3 1.000 0.040 4 105710713 intron variant A/G snv 4.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11731417
rs11731417
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105824855 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs12213892
rs12213892
ADGRG6
2 6 142381097 intron variant A/G snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs12441227
rs12441227
THSD4
3 15 71404547 intron variant A/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs12614274
rs12614274
LINC01807 ; LOC105373919
2 2 228719134 intron variant A/G snv 7.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs12664563
rs12664563 		2 6 142464064 intergenic variant A/G snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs13118928
rs13118928 		7 0.925 0.040 4 144565237 intron variant A/G snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs1441361
rs1441361
THSD4
2 15 71332783 intron variant A/G snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs16825247
rs16825247
LINC01807
2 2 228659425 intron variant A/G snv 7.3E-02 0.700 1.000 1 2010 2010
dbSNP: rs16909898
rs16909898
PTCH1 ; LOC100507346
4 9 95468726 intron variant A/G snv 8.4E-02 0.10 0.700 1.000 1 2010 2010
dbSNP: rs17036076
rs17036076
ARHGEF38
2 4 105654112 synonymous variant A/G snv 4.7E-02 5.0E-02 0.700 1.000 1 2010 2010
dbSNP: rs2282041
rs2282041
PTCH1
2 9 95486105 intron variant A/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs2637266
rs2637266 		2 10 76571560 intergenic variant A/G snv 0.48 0.700 1.000 1 2014 2014
dbSNP: rs3748069
rs3748069
ADGRG6
4 6 142446496 downstream gene variant A/G snv 0.39 0.700 1.000 1 2010 2010
dbSNP: rs3817928
rs3817928
ADGRG6
4 6 142429379 intron variant A/G snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs6830970
rs6830970
FAM13A
5 1.000 0.040 4 88855930 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs6903823
rs6903823
ZSCAN31 ; ZKSCAN3
4 6 28354519 intron variant A/G snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs6909857
rs6909857
ADGRG6
2 6 142380021 intron variant A/G snv 0.41 0.700 1.000 1 2010 2010
dbSNP: rs6922607
rs6922607
ADGRG6
3 6 142382346 intron variant A/G snv 0.22 0.700 1.000 1 2010 2010