rs6759709, MYT1L

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 2 2043625 intron variant A/G snv 0.28 0.700 1.000 1 2019 2019