Gene: C2 ×
Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1042663
rs1042663
C2 ; CYP21A2 ; C2-AS1
2 0.925 0.160 6 31937353 synonymous variant G/A snv 9.7E-02 0.12 0.700 1.000 3 2007 2011
dbSNP: rs2734335
rs2734335
C2 ; CYP21A2
1 1.000 0.120 6 31926167 intron variant G/A snv 0.53 0.700 1.000 3 2007 2011
dbSNP: rs550605
rs550605
C2 ; CYP21A2 ; C2-AS1
2 0.925 0.160 6 31939370 intron variant T/C snv 9.7E-02 0.12 0.700 1.000 3 2007 2011
dbSNP: rs659445
rs659445
C2 ; CYP21A2 ; EHMT2
3 0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 0.700 1.000 3 2007 2011
dbSNP: rs558702
rs558702
C2 ; CYP21A2 ; ZBTB12
6 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 0.700 1.000 2 2007 2011
dbSNP: rs497239
rs497239
C2 ; CYP21A2 ; C2-AS1
1 1.000 0.120 6 31940984 intron variant T/C snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs497309
rs497309
C2 ; CYP21A2
1 0.882 0.240 6 31924707 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs498240
rs498240
C2 ; CYP21A2
1 1.000 0.120 6 31924815 intron variant G/A snv 7.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs511294
rs511294
C2 ; CYP21A2
1 1.000 0.120 6 31921092 intron variant T/G snv 7.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs544167
rs544167
C2 ; CYP21A2
2 0.925 0.160 6 31922381 intron variant T/G snv 7.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs609061
rs609061
C2 ; CYP21A2 ; C2-AS1
1 1.000 0.120 6 31942385 intron variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs621701
rs621701
C2 ; CYP21A2 ; C2-AS1
1 1.000 0.120 6 31935344 non coding transcript exon variant G/A snv 7.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs644045
rs644045
C2 ; CYP21A2
2 0.851 0.240 6 31916180 intron variant A/G snv 0.72 0.700 1.000 1 2011 2011