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: rs11065774
rs11065774
MYL2
1 1.000 0.040 12 110917522 intron variant G/A snv 4.7E-02 0.700 1.000 1 2011 2011