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: rs12466022
rs12466022
LINC02580 ; LOC105374570
1.000 0.080 2 43131922 non coding transcript exon variant C/A;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs6718520
rs6718520
LINC02580
1.000 0.080 2 43098432 intron variant A/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs148550456
rs148550456
LINC02580 ; LOC105374570
2 43124884 intron variant ACAC/-;AC;ACACAC;ACACACAC delins
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs148550456
rs148550456
LINC02580 ; LOC105374570
2 43124884 intron variant ACAC/-;AC;ACACAC;ACACACAC delins
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs3179891
rs3179891
LINC02580
1.000 0.160 2 43092840 intron variant G/A snv 0.27
CUI: C0235280
Disease: Ototoxicity
Ototoxicity 		0.700 1.000 1 2017 2017