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: rs10906142
rs10906142
1 10 12396784 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs4747982
rs4747982
1 10 12393396 intron variant G/A snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs4750211
rs4750211
2 10 12393380 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012