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: rs67828806
rs67828806
COL1A1
2 1.000 0.200 17 50198177 missense variant C/G;T snv 0.700 0
dbSNP: rs72667037
rs72667037
COL1A1
2 1.000 0.120 17 50197767 missense variant C/A snv 0.700 0