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: rs34712979
rs34712979
5 1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17 0.700 1.000 3 2015 2019
dbSNP: rs6856422
rs6856422
1 4 105920805 intron variant G/T snv 0.59 0.700 1.000 1 2015 2015
dbSNP: rs7664805
rs7664805
1 4 105922801 intron variant G/A;C snv 0.700 1.000 1 2015 2015