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: rs10419408
rs10419408
2 19 12831936 intron variant A/G snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs10426080
rs10426080
2 19 12847036 intron variant A/G snv 0.40 0.700 1.000 1 2009 2009
dbSNP: rs1078264
rs1078264
2 19 12852329 splice region variant T/C snv 0.34 0.35 0.700 1.000 1 2009 2009
dbSNP: rs11671604
rs11671604
2 19 12820875 intron variant A/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs117062702
rs117062702
1 19 12871477 intron variant C/G;T snv 8.9E-04 0.700 1.000 1 2018 2018
dbSNP: rs2242512
rs2242512
2 19 12864785 intron variant G/A;T snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2242514
rs2242514
2 19 12871984 intron variant A/G snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2290688
rs2290688
2 19 12847883 synonymous variant T/C snv 0.36 0.40 0.700 1.000 1 2009 2009
dbSNP: rs2290689
rs2290689
2 19 12847546 intron variant T/C snv 0.40 0.700 1.000 1 2009 2009
dbSNP: rs4614850
rs4614850
2 19 12863822 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs4804737
rs4804737
2 19 12837124 intron variant T/C snv 0.40 0.700 1.000 1 2009 2009