Source: GWASCAT

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: rs11969064
rs11969064 		6 18104864 intergenic variant C/T snv 0.11
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs11969064
rs11969064 		6 18104864 intergenic variant C/T snv 0.11
CUI: C0854467
Disease: Myelosuppression
Myelosuppression 		0.700 1.000 1 2019 2019