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: rs797045167
rs797045167
SOS2
1 1.000 14 50182521 missense variant A/C;G;T snv 0.800 1.000 2 2015 2015
dbSNP: rs869320687
rs869320687
SOS2
2 0.925 0.160 14 50161551 missense variant G/C snv 0.800 0
dbSNP: rs1442962879
rs1442962879
SOS2
1 1.000 14 50130563 missense variant G/A snv 1.2E-05 7.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs373233749
rs373233749
SOS2
1 1.000 14 50174521 missense variant C/T snv 2.8E-05 7.0E-06 0.700 1.000 1 2015 2015