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: rs10037512
rs10037512
3 5 89058858 intron variant T/A;C snv 0.700 1.000 2 2010 2015
dbSNP: rs1366594
rs1366594
3 5 89080244 intron variant A/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs2217257
rs2217257
1 5 89046775 intron variant C/T snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs34957094
rs34957094
1 5 88979517 intron variant -/C ins 2.0E-05 0.700 1.000 1 2017 2017
dbSNP: rs6894139
rs6894139
3 5 89031965 non coding transcript exon variant T/G snv 0.57 0.700 1.000 1 2014 2014