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: rs10813766
rs10813766
1 9 331490 intron variant T/G snv 0.64 0.800 1.000 1 2011 2011
dbSNP: rs2992836
rs2992836
1 9 276053 intron variant G/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs3215853
rs3215853
1 9 273178 intron variant -/A delins 0.72 0.700 1.000 1 2016 2016
dbSNP: rs471756
rs471756
1 9 239313 intron variant G/C snv 0.57 0.700 1.000 1 2016 2016
dbSNP: rs56318916
rs56318916
2 9 329344 intron variant A/- del 0.22 0.700 1.000 1 2016 2016
dbSNP: rs7869524
rs7869524
1 9 341829 intron variant G/T snv 0.52 0.700 1.000 1 2016 2016