Gene: BNC2 ×
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: rs10756785
rs10756785
BNC2
2 0.925 0.040 9 16700839 intron variant C/T snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs3904778
rs3904778
BNC2
3 0.882 0.200 9 16681995 intron variant C/G snv 0.62 0.700 1.000 1 2015 2015
dbSNP: rs7028900
rs7028900
BNC2
2 0.925 0.040 9 16690614 intron variant G/C snv 0.61 0.700 1.000 1 2019 2019