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: rs2393967
rs2393967
3 10 63373396 intron variant A/C snv 0.23 0.800 1.000 2 2009 2012
dbSNP: rs7075195
rs7075195
1 10 63290899 intron variant A/G snv 0.38 0.800 1.000 2 2011 2014
dbSNP: rs10761741
rs10761741
4 1.000 0.040 10 63306426 intron variant G/T snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs4379723
rs4379723
2 10 63203689 intron variant T/C snv 0.43 0.700 1.000 1 2014 2014
dbSNP: rs7896518
rs7896518
5 10 63344740 intron variant A/G snv 0.38 0.700 1.000 1 2012 2012