Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs782627671
rs782627671
RPS19 ; MIR6797
1.000 0.040 19 41869159 missense variant C/T snv 4.0E-06
CUI: C0836924
Disease: Thrombocytosis
Thrombocytosis 		0.010 1.000 1 2018 2018
dbSNP: rs782627671
rs782627671
RPS19 ; MIR6797
1.000 0.040 19 41869159 missense variant C/T snv 4.0E-06
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2018 2018