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: rs2844573
rs2844573 		3 0.882 0.160 6 31367677 intron variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs9263726
rs9263726
PSORS1C1 ; PSORS1C2
1 1.000 0.040 6 31138722 missense variant G/A snv 0.11 0.14 0.010 1.000 1 2019 2019