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: rs267606825
rs267606825
TTLL5 ; FLVCR2
2 0.925 0.160 14 75641008 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2016 2016