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: rs11921187
rs11921187
1 3 133832798 intron variant T/C snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12637730
rs12637730
3 3 133827453 3 prime UTR variant C/T snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs17310798
rs17310798
1 3 133844095 intron variant T/C snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs1880663
rs1880663
1 3 133862615 intron variant A/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs2293374
rs2293374
1 3 133828401 3 prime UTR variant G/A snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs2692672
rs2692672
1 3 133836656 intron variant T/G snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs6793673
rs6793673
1 3 133834428 intron variant C/T snv 0.14 0.700 1.000 1 2011 2011