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: rs10173717
rs10173717
MTLN
1 1.000 0.080 2 110225473 intron variant A/G snv 0.29 0.010 1.000 1 2013 2013