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: rs11634257
rs11634257
BMF
1 15 40096291 intron variant T/A snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs34245505
rs34245505
BMF
1 15 40104990 intron variant C/G snv 0.14 0.700 1.000 1 2019 2019