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: rs880315
rs880315
9 0.925 0.120 1 10736809 intron variant T/C snv 0.32 0.700 1.000 8 2011 2018
dbSNP: rs17035646
rs17035646
6 1 10736490 intron variant G/A;T snv 0.700 1.000 3 2018 2019
dbSNP: rs12046278
rs12046278
3 1 10739520 intron variant T/C snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs35295665
rs35295665
2 1 10737371 intron variant -/C delins 0.700 1.000 1 2018 2018