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: rs5743467
rs5743467
DEFB1
3 0.925 0.040 8 6874007 intron variant C/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs61475845
rs61475845
CNTN5
2 1.000 0.040 11 99948244 intron variant G/A snv 2.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs982422
rs982422 		2 1.000 0.040 12 78453479 intron variant G/T snv 0.26 0.700 1.000 1 2018 2018