MYO1D, myosin ID, 4642

N. diseases: 16; N. variants: 11
Disease: Reticulocyte count (procedure) ×
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: rs112916054
rs112916054 		17 32797244 intron variant C/T snv 0.14
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs17183628
rs17183628 		17 32857613 intron variant T/C snv 0.14
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs17780981
rs17780981 		17 32792019 intron variant A/G snv 0.14
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs62070183
rs62070183 		17 32837349 intron variant T/C snv 0.14
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016