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: rs2440238
rs2440238
2 11 31886440 non coding transcript exon variant T/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs597660
rs597660
2 11 31893668 intron variant G/T snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs602074
rs602074
3 1.000 0.040 11 31900616 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs602907
rs602907
2 11 31900468 intron variant T/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs621420
rs621420
2 11 31897652 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs623102
rs623102
2 11 31904890 intron variant C/A snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs623312
rs623312
2 11 31885918 non coding transcript exon variant G/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs652722
rs652722
4 1.000 0.040 11 31883988 intron variant C/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs666822
rs666822
2 11 31895723 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs667156
rs667156
2 11 31895673 intron variant T/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs673946
rs673946
2 11 31896053 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs683028
rs683028
3 1.000 0.040 11 31901029 intron variant A/G snv 0.44 0.700 1.000 1 2012 2012