Gene: PRXL2C ×
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: rs151326868
rs151326868
PRXL2C
1 1.000 0.040 9 96641842 missense variant G/A;C snv 4.2E-04 7.3E-04 0.010 1.000 1 2018 2018