MYO1D, myosin ID, 4642

N. diseases: 16; N. variants: 11
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17183295
rs17183295
1.000 17 32751254 intron variant C/T snv 0.14
Red cell distribution width determination
0.700 1.000 1 2016 2016
dbSNP: rs62068432
rs62068432
17 32739479 intron variant A/G snv 0.16
Red cell distribution width determination
0.700 1.000 1 2019 2019