Source: GWASDB

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: rs2072633
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs438999
rs438999
CYP21A2 ; SKIV2L ; NELFE
0.925 0.160 6 31960529 missense variant A/G snv 9.7E-02 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs403569
rs403569
CYP21A2 ; NELFE ; MIR1236
1.000 0.120 6 31957103 intron variant G/A snv 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs419788
rs419788
CYP21A2 ; SKIV2L ; NELFE
1.000 0.120 6 31961022 intron variant T/A;C snv 0.76
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs440454
rs440454
CYP21A2 ; SKIV2L ; NELFE
1.000 0.120 6 31959565 non coding transcript exon variant A/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs522162
rs522162
CFB ; CYP21A2 ; NELFE
0.925 0.160 6 31952140 3 prime UTR variant T/C snv 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs550513
rs550513
CYP21A2 ; NELFE
0.925 0.160 6 31952910 intron variant C/T snv 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011
dbSNP: rs760070
rs760070
CFB ; CYP21A2 ; NELFE
0.882 0.280 6 31952179 3 prime UTR variant T/C snv 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2011 2011