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: rs11715464
rs11715464
1 3 42868195 intron variant A/G snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1366046
rs1366046
1 3 42867283 3 prime UTR variant A/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs2228468
rs2228468
6 0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 0.700 1.000 1 2012 2012
dbSNP: rs3919627
rs3919627
2 3 42867668 intron variant G/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs7612912
rs7612912
1 3 42869129 intron variant T/C snv 0.39 0.700 1.000 1 2012 2012