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: rs1057519043
rs1057519043
FGFR2
4 0.851 0.120 10 121517391 missense variant C/A;G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs28931615
rs28931615
FGFR3
13 0.732 0.240 4 1804426 missense variant C/A;T snv 0.020 1.000 2 1996 2019
dbSNP: rs121913474
rs121913474
FGFR2
9 0.790 0.200 10 121515260 missense variant A/G snv 0.010 1.000 1 2019 2019
dbSNP: rs121918505
rs121918505
FGFR2
5 0.851 0.080 10 121520119 missense variant A/G snv 0.010 1.000 1 2019 2019