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: rs10806425
rs10806425
BACH2
6 0.851 0.280 6 90216893 intron variant C/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs116446171
rs116446171 		4 0.851 0.160 6 484453 downstream gene variant C/G snv 2.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs13254990
rs13254990
PVT1
4 0.882 0.120 8 128064205 intron variant C/T snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs2395192
rs2395192 		1 1.000 0.120 6 32479867 intergenic variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs41289586
rs41289586
ANO10
3 0.882 0.160 3 43577066 missense variant C/T snv 1.8E-02 1.9E-02 0.700 1.000 1 2019 2019