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: rs727503260
rs727503260
4 0.851 0.080 14 23425403 missense variant C/G;T snv 0.700 1.000 10 2003 2015
dbSNP: rs397516153
rs397516153
2 0.925 0.040 14 23424935 missense variant G/A;T snv 0.700 1.000 2 2008 2017
dbSNP: rs727503244
rs727503244
1 1.000 0.040 14 23417573 missense variant A/G snv 4.4E-05 5.6E-05 0.700 1.000 1 2010 2010
dbSNP: rs727503269
rs727503269
3 0.882 0.040 14 23429329 missense variant T/C snv 0.700 0