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: rs1553517323
rs1553517323
COL5A2
4 1.000 2 189085204 missense variant C/A snv 0.700 0
dbSNP: rs1554846212
rs1554846212
KAT6B ; DUPD1
9 0.851 0.160 10 75030037 missense variant C/T snv 0.700 0