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: rs935058009
rs935058009
TPO
1 1.000 0.120 2 1503983 missense variant T/C snv 0.700 0
dbSNP: rs146351101
rs146351101
TPO
1 1.000 0.120 2 1504076 missense variant G/A snv 6.0E-05 2.1E-05 0.700 1.000 17 1995 2016