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: rs60600003
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs60600003
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs60600003
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs60600003
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs60600003
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs60600003
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs60600003
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019