Source: ALL
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: rs11212617
rs11212617
C11orf65
7 0.827 0.200 11 108412434 intron variant C/A snv 0.49 0.700 1.000 2 2011 2011
dbSNP: rs12787445
rs12787445
NPAT
1 11 108163397 intron variant A/G snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs183460
rs183460
NPAT
1 11 108219983 intron variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs227041
rs227041
ATM ; C11orf65
1 11 108352074 intron variant C/A snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs227073
rs227073
ATM ; C11orf65
1 11 108341965 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs227077
rs227077
C11orf65
1 11 108382525 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs228591
rs228591
ATM
1 11 108226606 5 prime UTR variant A/G snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs419716
rs419716
ATM ; C11orf65
1 11 108350372 intron variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs573890
rs573890
C11orf65
1 11 108380636 intron variant C/G;T snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs609557
rs609557
NPAT
1 11 108213786 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs624366
rs624366
ATM
6 0.827 0.120 11 108283370 intron variant G/C snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs645485
rs645485
ATM
1 11 108298136 intron variant A/G snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs6589007
rs6589007
NPAT
1 11 108169377 intron variant A/G snv 0.55 0.700 1.000 1 2011 2011
dbSNP: rs7931930
rs7931930
C11orf65
1 11 108397559 intron variant G/T snv 0.49 0.700 1.000 1 2011 2011