rs1377817, MYH14

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Platinum measurement
CUI: C0202455
Disease: Platinum measurement
7 19 50300809 intron variant T/G snv 0.15 0.700 1.000 1 2019 2019