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: rs4950806
rs4950806
1 1 201983446 5 prime UTR variant T/C snv 0.58 0.60 0.800 1.000 1 2011 2011
dbSNP: rs10800805
rs10800805
1 1 201990610 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11586632
rs11586632
1 1 201986486 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11590299
rs11590299
1 1 201984468 intron variant T/A snv 0.55 0.700 1.000 1 2011 2011
dbSNP: rs4950752
rs4950752
1 1 201987299 intron variant G/A snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs6689324
rs6689324
1 1 201985569 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs7529387
rs7529387
1 1 201980910 upstream gene variant G/A snv 0.58 0.700 1.000 1 2011 2011