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: rs587777100
rs587777100
C15orf41
1 1.000 15 36697379 missense variant T/A snv 0.800 1.000 3 2013 2019
dbSNP: rs587777101
rs587777101
C15orf41
1 1.000 15 36657840 missense variant A/C;G snv 2.4E-05 0.800 1.000 3 2013 2019
dbSNP: rs768744226
rs768744226
C15orf41
1 1.000 15 36709952 missense variant A/G snv 1.6E-05 0.700 1.000 3 2013 2019