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: rs2835872
rs2835872
3 1.000 0.080 21 37654970 intron variant G/A snv 0.26 0.800 1.000 1 2012 2012
dbSNP: rs10483038
rs10483038
3 1.000 0.080 21 37652469 intron variant T/C snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs111372083
rs111372083
3 1.000 0.080 21 37638374 intron variant C/A;T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs111576572
rs111576572
3 1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs12482570
rs12482570
3 1.000 0.080 21 37705475 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs1399590
rs1399590
3 1.000 0.080 21 37681768 intron variant G/A snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs1399591
rs1399591
3 1.000 0.080 21 37681654 intron variant C/T snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs1399592
rs1399592
3 1.000 0.080 21 37681559 intron variant T/A;G snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs1475839
rs1475839
3 1.000 0.080 21 37649639 intron variant C/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs1515050
rs1515050
3 1.000 0.080 21 37630840 intron variant T/C snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs1515056
rs1515056
3 1.000 0.080 21 37710283 intron variant C/G;T snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1709817
rs1709817
3 1.000 0.080 21 37664047 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1709818
rs1709818
3 1.000 0.080 21 37663909 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1709819
rs1709819
3 1.000 0.080 21 37663813 intron variant A/C snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs1709820
rs1709820
3 1.000 0.080 21 37663669 intron variant A/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1709826
rs1709826
3 1.000 0.080 21 37677171 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1709832
rs1709832
3 1.000 0.080 21 37665865 intron variant T/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1709833
rs1709833
3 1.000 0.080 21 37665503 intron variant A/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1709835
rs1709835
3 1.000 0.080 21 37665334 intron variant A/C;G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs17814920
rs17814920
3 1.000 0.080 21 37643595 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1787330
rs1787330
3 1.000 0.080 21 37630485 intron variant G/A snv 0.74 0.700 1.000 1 2012 2012
dbSNP: rs1787331
rs1787331
3 1.000 0.080 21 37631223 intron variant T/G snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs1787394
rs1787394
3 1.000 0.080 21 37663874 intron variant C/A snv 0.58 0.700 1.000 1 2012 2012
dbSNP: rs1787395
rs1787395
3 1.000 0.080 21 37664176 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1787396
rs1787396
3 1.000 0.080 21 37664185 intron variant A/C snv 0.57 0.700 1.000 1 2012 2012