Source: ALL
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: rs387906750
rs387906750
AKR1C2
1 1.000 0.160 10 5001531 missense variant T/C snv 0.800 1.000 1 2011 2011
dbSNP: rs387906751
rs387906751
AKR1C2
1 1.000 0.160 10 4991861 missense variant T/G snv 0.800 1.000 1 2011 2011
dbSNP: rs797044460
rs797044460
AKR1C2
1 1.000 0.160 10 5000649 missense variant A/C snv 0.800 0
dbSNP: rs13222
rs13222
AKR1C2 ; LOC101928051
1 1.000 0.160 10 4995770 missense variant A/C;G snv 2.4E-04 1.9E-02 0.700 0
dbSNP: rs398122815
rs398122815
AKR1C4
1 1.000 0.160 10 5200075 intron variant G/T snv 0.700 0