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: rs2293088
rs2293088 		1 151805175 intron variant G/A snv 0.28
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1521179
rs1521179 		1.000 0.040 1 151800911 3 prime UTR variant G/A snv 0.10 5.3E-02
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs61746299
rs61746299 		1.000 0.040 1 151801375 missense variant T/A;C snv 9.9E-02; 4.0E-06
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		Nervous System Diseases 0.010 < 0.001 1 2012 2012