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: rs1057519849
rs1057519849
1 8 127738386 missense variant C/T snv 0.700 1.000 1 2014 2014
dbSNP: rs1057519850
rs1057519850
1 8 127738447 missense variant C/T snv 0.700 1.000 1 2014 2014
dbSNP: rs1057519851
rs1057519851
MYC
1 8 127738995 missense variant C/G snv 0.700 1.000 1 2014 2014
dbSNP: rs121918683
rs121918683
2 1.000 0.160 8 127738519 missense variant A/C snv 0.700 1.000 1 2014 2014
dbSNP: rs756091827
rs756091827
6 0.851 0.200 8 127738435 missense variant C/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs775522201
rs775522201
1 8 127738393 missense variant C/T snv 0.700 1.000 1 2014 2014
dbSNP: rs28933407
rs28933407
2 1.000 0.160 8 127738431 missense variant C/T snv 0.010 1.000 1 2015 2015