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: rs1553433412
rs1553433412
TPRKB
1 1.000 2 73730594 missense variant A/G snv 0.800 1.000 1 2017 2017
dbSNP: rs1233885358
rs1233885358
TPRKB
1 1.000 2 73730025 missense variant T/C snv 7.0E-06 0.800 0