Gene: CYP21A2 ×
Source: UNIPROT ×
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: rs781074931
rs781074931
CYP21A2
1 1.000 0.200 6 32040574 missense variant C/A;T snv 4.1E-06; 6.1E-05 0.700 1.000 20 1985 2016
dbSNP: rs111647200
rs111647200
CYP21A2 ; CYP21A1P
1 1.000 0.200 6 32007071 non coding transcript exon variant A/G;T snv 1.4E-05 0.700 0
dbSNP: rs1330554738
rs1330554738
CYP21A2
1 0.925 0.200 6 32040562 missense variant C/T snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs1333278223
rs1333278223
CYP21A2
1 1.000 0.200 6 32038752 missense variant T/C snv 7.0E-06 0.700 0
dbSNP: rs1413433421
rs1413433421
CYP21A2
1 1.000 0.200 6 32038591 missense variant G/A snv 6.0E-06 0.700 0
dbSNP: rs184649564
rs184649564
CYP21A2 ; TNXB
1 1.000 0.200 6 32041085 missense variant G/A;T snv 1.9E-05; 4.9E-03 0.700 0
dbSNP: rs750337015
rs750337015
CYP21A2
1 1.000 0.200 6 32040051 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs765001985
rs765001985
CYP21A2
1 1.000 0.200 6 32040167 missense variant C/T snv 4.1E-06 0.700 0
dbSNP: rs767333157
rs767333157
CYP21A2 ; TNXB
1 1.000 0.200 6 32040952 missense variant C/T snv 2.1E-03 7.3E-04 0.700 0
dbSNP: rs772900496
rs772900496
CYP21A2
1 1.000 0.200 6 32040529 missense variant C/T snv 2.1E-05 0.700 0
dbSNP: rs957886272
rs957886272
CYP21A2
1 1.000 0.200 6 32039124 missense variant T/A;G snv 4.1E-06 0.700 0