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: rs255049
rs255049
3 1.000 0.040 16 67979568 intron variant T/C snv 0.34 0.800 1.000 2 2009 2019
dbSNP: rs255056
rs255056
2 16 67982282 upstream gene variant G/C snv 0.17 0.700 1.000 1 2019 2019