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: rs34164109
rs34164109
2 6 135100038 intron variant C/T snv 0.22 0.700 1.000 1 2016 2016
dbSNP: rs9389248
rs9389248
2 6 134961518 3 prime UTR variant T/C snv 0.45 0.700 1.000 1 2016 2016
dbSNP: rs9402673
rs9402673
1 6 135001482 intron variant C/T snv 0.43 0.700 1.000 1 2016 2016