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: rs1554100963
rs1554100963
FOXC1
2 0.925 0.080 6 1610852 inframe deletion GTC/- delins 0.700 0
dbSNP: rs1201848305
rs1201848305
FGFR2
1 1.000 0.080 10 121503933 synonymous variant A/G snv 1.2E-05 0.010 1.000 1 2005 2005
dbSNP: rs121918491
rs121918491
FGFR2
15 0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2005 2005