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: rs108499
rs108499
2 11 61779765 intron variant C/T snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs149803
rs149803
2 11 61771548 synonymous variant C/G;T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs174528
rs174528
5 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 1 2011 2011
dbSNP: rs174532
rs174532
2 11 61781402 intron variant G/A snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs174534
rs174534
3 1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs174535
rs174535
19 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 0.700 1.000 1 2011 2011
dbSNP: rs174536
rs174536
3 11 61784455 non coding transcript exon variant A/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs17762402
rs17762402
2 11 61785729 intron variant G/A snv 4.8E-02 0.700 1.000 1 2011 2011
dbSNP: rs2269928
rs2269928
2 11 61770057 intron variant T/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs509360
rs509360
3 11 61781087 intron variant A/G snv 0.61 0.52 0.700 1.000 1 2011 2011
dbSNP: rs579383
rs579383
2 11 61769111 intron variant G/A snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs650436
rs650436
2 11 61768958 intron variant C/T snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs102275
rs102275
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.800 1.000 3 2011 2013
dbSNP: rs740006
rs740006
2 11 61790396 3 prime UTR variant T/C snv 7.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs695867
rs695867
1 11 61793816 intron variant A/G snv 2.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs174538
rs174538
21 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 0.700 1.000 1 2011 2011
dbSNP: rs412334
rs412334
2 11 61792789 5 prime UTR variant C/T snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs7102974
rs7102974
1 11 61792563 5 prime UTR variant C/T snv 8.5E-03 9.6E-03 0.700 1.000 1 2011 2011