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: rs182087722
rs182087722
2 1.000 0.040 6 28044305 intron variant A/G snv 5.8E-03 0.700 1.000 1 2017 2017
dbSNP: rs202906
rs202906
2 1.000 0.040 6 28043874 intron variant T/C snv 0.13 0.700 1.000 1 2017 2017