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: rs11066453
rs11066453
OAS1
4 1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs12229654
rs12229654 		20 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs12539316
rs12539316 		6 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs2074356
rs2074356
HECTD4
18 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs2393791
rs2393791
HNF1A
8 0.925 0.160 12 120986153 intron variant C/T snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs4820599
rs4820599
GGT1 ; LRRC75B
6 0.925 0.160 22 24594246 intron variant A/G snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs4835265
rs4835265
ZNF827
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 1 2011 2011