Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1801516
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11
CUI: C0025202
Disease: melanoma
melanoma 		0.810 1.000 1 2011 2017
dbSNP: rs227041
rs227041
ATM ; C11orf65
11 108352074 intron variant C/A snv 0.52
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs227073
rs227073
ATM ; C11orf65
11 108341965 intron variant G/A;C;T snv
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs228591
rs228591
ATM
11 108226606 5 prime UTR variant A/G snv 0.54
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs3218688
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3218688
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3218688
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3218688
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs419716
rs419716
ATM ; C11orf65
11 108350372 intron variant A/C;T snv
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs4987897
rs4987897
ATM
11 108227415 5 prime UTR variant C/T snv 1.4E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4987897
rs4987897
ATM
11 108227415 5 prime UTR variant C/T snv 1.4E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs624366
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011
dbSNP: rs645485
rs645485
ATM
11 108298136 intron variant A/G snv 0.54
CUI: C3547187
Disease: response to metformin
response to metformin 		0.700 1.000 1 2011 2011