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: rs76895963
rs76895963
6 1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 0.700 1.000 3 2017 2019
dbSNP: rs71061176
rs71061176
1 12 4269579 intron variant -/T ins 0.18 0.700 1.000 1 2019 2019