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: rs1052553
rs1052553
8 0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 0.700 1.000 1 2015 2015
dbSNP: rs1053924
rs1053924
1 1.000 0.120 6 32152938 non coding transcript exon variant T/C snv 0.71 0.700 1.000 1 2007 2007
dbSNP: rs1055271
rs1055271
1 1.000 0.120 22 50489911 3 prime UTR variant G/C snv 0.27 0.010 1.000 1 2011 2011
dbSNP: rs1055569
rs1055569
3 0.882 0.240 6 31472305 non coding transcript exon variant C/T snv 0.41 0.700 1.000 1 2007 2007
dbSNP: rs1058026
rs1058026
5 0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 0.700 1.000 1 2007 2007
dbSNP: rs1063856
rs1063856
VWF
14 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2000 2000
dbSNP: rs1065356
rs1065356
1 1.000 0.120 6 31719231 synonymous variant G/A snv 0.27 0.31 0.700 1.000 1 2007 2007
dbSNP: rs10735810
rs10735810
VDR
26 0.662 0.640 12 47879112 start lost A/C;G;T snv 0.050 1.000 5 2008 2015
dbSNP: rs10741657
rs10741657
34 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 < 0.001 1 2007 2007
dbSNP: rs10743152
rs10743152
TH
1 1.000 0.120 11 2174751 upstream gene variant T/C snv 0.63 0.700 1.000 1 2007 2007
dbSNP: rs10758593
rs10758593
8 0.827 0.240 9 4292083 intron variant G/A snv 0.45 0.710 0.500 2 2011 2017
dbSNP: rs10766196
rs10766196
2 0.925 0.120 11 14891585 5 prime UTR variant A/G snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs10770125
rs10770125
4 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 0.010 1.000 1 2013 2013
dbSNP: rs10770141
rs10770141
2 1.000 0.120 11 2172610 upstream gene variant A/C;G snv 0.700 1.000 1 2007 2007
dbSNP: rs1077393
rs1077393
3 0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 0.700 1.000 1 2007 2007
dbSNP: rs10774654
rs10774654
1 1.000 0.120 12 112525756 intergenic variant A/G snv 0.20 0.700 1.000 1 2008 2008
dbSNP: rs10774671
rs10774671
14 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 0.030 0.667 3 2006 2009
dbSNP: rs10786436
rs10786436
1 1.000 0.120 10 98540425 intron variant C/T snv 0.40 0.800 1.000 1 2011 2011
dbSNP: rs10795791
rs10795791
2 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 0.700 1.000 1 2015 2015
dbSNP: rs10807113
rs10807113
1 1.000 0.120 6 32754409 upstream gene variant C/A;G snv 0.700 1.000 1 2007 2007
dbSNP: rs10810632
rs10810632
1 1.000 0.120 9 16789026 intron variant C/T snv 0.85 0.700 1.000 1 2010 2010
dbSNP: rs10811661
rs10811661
22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.010 1.000 1 2012 2012
dbSNP: rs10822050
rs10822050
14 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10850053
rs10850053
1 1.000 0.120 12 112539973 regulatory region variant T/C snv 0.19 0.700 1.000 1 2008 2008
dbSNP: rs10889677
rs10889677
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 < 0.001 1 2013 2013