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: rs11915082
rs11915082
2 3 196082268 regulatory region variant G/A snp 0.30 0.800 3 2009 2017
dbSNP: rs11185506
rs11185506
3 3 196070705 intron variant G/A,C snp 0.47 0.700 1 2012 2012
dbSNP: rs13072608
rs13072608
3 3 196073396 intron variant C/T snp 0.48 0.700 1 2012 2012
dbSNP: rs2284889
rs2284889
3 3 196061376 intron variant G/A snp 0.48 0.700 1 2012 2012
dbSNP: rs2284890
rs2284890
3 3 196061276 intron variant T/C snp 0.48 0.700 1 2012 2012
dbSNP: rs2300774
rs2300774
3 3 196066841 intron variant G/A snp 0.48 0.700 1 2012 2012
dbSNP: rs2300780
rs2300780
2 3 196063420 non coding transcript exon variant T/A,C snp 0.48 0.700 1 2012 2012
dbSNP: rs3326
rs3326
3 3 196054635 intron variant G/A snp 0.29 0.700 1 2012 2012
dbSNP: rs3761717
rs3761717
3 3 196071076 intron variant G/C snp 0.48 0.700 1 2012 2012
dbSNP: rs3789135
rs3789135
2 3 196065999 intron variant C/A snp 0.44 0.700 1 2017 2017
dbSNP: rs3804139
rs3804139
3 3 196080754 intron variant T/C snp 0.48 0.700 1 2012 2012
dbSNP: rs3817672
rs3817672
8 0.821 0.250 3 196073940 missense variant C/T snp 0.45 0.42 0.700 1 2012 2012
dbSNP: rs3933
rs3933
2 3 196058126 non coding transcript exon variant G/A snp 0.32 0.700 1 2012 2012
dbSNP: rs406271
rs406271
2 3 196050105 3 prime UTR variant T/C snp 0.32 0.700 1 2012 2012
dbSNP: rs454516
rs454516
2 3 196066524 intron variant G/C snp 0.18 0.700 1 2012 2012
dbSNP: rs4927866
rs4927866
2 3 196069178 intron variant G/T snp 0.18 0.700 1 2012 2012
dbSNP: rs557527
rs557527
2 3 196053838 intron variant G/A snp 0.32 0.700 1 2012 2012
dbSNP: rs6583288
rs6583288
2 3 196082693 regulatory region variant A/G snp 0.18 0.700 1 2012 2012
dbSNP: rs714602
rs714602
2 3 196067108 intron variant T/C snp 0.29 0.700 1 2012 2012
dbSNP: rs9846149
rs9846149
3 3 196060437 non coding transcript exon variant C/G snp 0.48 0.700 1 2012 2012
dbSNP: rs9858727
rs9858727
3 3 196067370 intron variant A/T snp 0.48 0.700 1 2012 2012
dbSNP: rs9859260
rs9859260
3 3 196073676 intron variant C/A,T snp 0.48 0.700 1 2012 2012
dbSNP: rs9859401
rs9859401
3 3 196073732 intron variant C/A,T snp 0.48 0.700 1 2012 2012