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: rs11855326
rs11855326
2 15 71318496 intron variant G/A snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs11858540
rs11858540
2 15 71330447 intron variant T/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs12441227
rs12441227
3 15 71404547 intron variant A/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs12899618
rs12899618
4 15 71352781 intron variant G/A snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs1441361
rs1441361
2 15 71332783 intron variant A/G snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs17786786
rs17786786
2 15 71316280 intron variant A/C snv 0.32 0.700 1.000 1 2014 2014
dbSNP: rs1837762
rs1837762
2 15 71319964 intron variant G/A snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs6494904
rs6494904
2 15 71317183 intron variant G/A snv 0.65 0.700 1.000 1 2014 2014
dbSNP: rs8033889
rs8033889
2 15 71387741 intron variant G/T snv 0.23 0.700 1.000 1 2014 2014