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: rs267606621
rs267606621
3 0.882 0.080 16 70268356 missense variant C/T snv 0.710 1.000 1 2012 2012
dbSNP: rs797044801
rs797044801
1 1.000 0.080 16 70254688 missense variant T/G snv 0.700 0