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: rs112190912
rs112190912
HBZ
2 16 146470 intron variant A/G snv 4.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs113613943
rs113613943
HBZ
1 16 151755 intron variant A/G snv 7.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs11864973
rs11864973
HBZ
4 16 143225 intron variant G/A;T snv 3.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs2974760
rs2974760
HBZ
2 16 152050 intron variant C/A snv 0.58 0.700 1.000 1 2016 2016