Source: BEFREE ×
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: rs1057519731
rs1057519731
1 0.925 0.040 15 66436816 missense variant G/C snv 0.720 1.000 2 2011 2014
dbSNP: rs397516792
rs397516792
1 0.827 0.280 15 66436825 missense variant C/A;G;T snv 0.720 1.000 2 2009 2015
dbSNP: rs1057519856
rs1057519856
1 0.925 0.040 15 66436815 missense variant T/A snv 0.020 1.000 2 2014 2014