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: rs10497655
rs10497655
2 1.000 0.040 2 184597314 intron variant T/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs34714481
rs34714481
1 1.000 0.040 2 184597742 intron variant A/G snv 0.12 0.010 1.000 1 2019 2019