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: rs354033
rs354033
1.000 0.080 7 149592373 intron variant G/A snv 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.800 1.000 1 2011 2011
dbSNP: rs117107603
rs117107603
7 149564734 intron variant C/A snv 1.9E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019