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: rs104893639
rs104893639
MATN3 ; LOC101928222
1 1.000 0.080 2 20003167 missense variant A/T snv 0.700 1.000 1 2004 2004