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: rs10491964
rs10491964
1 12 2391265 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12425203
rs12425203
1 12 2365495 intron variant C/T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs2239063
rs2239063
2 1.000 0.040 12 2402665 intron variant A/C snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs4765929
rs4765929
1 12 2409186 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs7312105
rs7312105
2 12 2414189 intron variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs7312107
rs7312107
1 12 2414204 intron variant A/G;T snv 0.700 1.000 1 2012 2012