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: rs59325236
rs59325236
RBFOX1
1 1.000 0.040 16 7706047 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs9271588
rs9271588 		6 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 0.700 1.000 1 2019 2019