Source: BEFREE

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: rs2297322
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.010 1.000 1 2019 2019
dbSNP: rs2297322
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2014 2014
dbSNP: rs2297322
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2009 2009
dbSNP: rs2297322
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2019 2019