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: rs10231520
rs10231520
1 1.000 0.040 7 20742471 intron variant C/T snv 0.29 0.010 1.000 1 2013 2013
dbSNP: rs17817117
rs17817117
1 1.000 0.040 7 20685203 intron variant G/C snv 0.29 0.010 1.000 1 2013 2013
dbSNP: rs2301641
rs2301641
1 1.000 0.040 7 20658647 missense variant A/G snv 0.33 0.40 0.010 1.000 1 2013 2013