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: rs1554333853
rs1554333853
CDK13
54 0.689 0.320 7 40046006 missense variant A/G snv 0.800 1.000 2 2016 2017
dbSNP: rs878853160
rs878853160
CDK13
5 0.882 0.120 7 40046007 missense variant A/G snv 0.800 1.000 2 2016 2017
dbSNP: rs1057519632
rs1057519632
CDK13
2 1.000 7 39999467 missense variant G/A snv 0.700 0
dbSNP: rs1057519633
rs1057519633
CDK13
1 1.000 7 39999458 missense variant G/C snv 0.700 0
dbSNP: rs1057519634
rs1057519634
CDK13
1 1.000 7 40001930 missense variant G/A snv 0.700 0
dbSNP: rs1064795731
rs1064795731
CDK13
1 1.000 7 40001878 missense variant A/G snv 0.700 0
dbSNP: rs1554317002
rs1554317002
CDK13 ; LOC112267983
45 0.724 0.440 7 39950821 frameshift variant C/- delins 0.700 0
dbSNP: rs1562722163
rs1562722163
CDK13
1 1.000 7 40001924 missense variant C/A snv 0.700 0