Source: ALL
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: rs2438321
rs2438321 		1 11 98629680 intergenic variant A/G snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs34459162
rs34459162
RCN3
3 1.000 0.040 19 49542659 missense variant T/A;C snv 4.4E-05; 7.8E-02 0.700 1.000 1 2018 2018