Source: CURATED

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: rs6731759
rs6731759
ALK
1.000 2 29804123 intron variant A/G snv 0.42
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 1 2019 2019
dbSNP: rs1057519784
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 3 2012 2014
dbSNP: rs1057519781
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 2 2012 2014
dbSNP: rs1057519782
rs1057519782
ALK
1.000 0.040 2 29220734 missense variant G/T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 2 2012 2014
dbSNP: rs863225281
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 2 2012 2014
dbSNP: rs1057519783
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2012 2012
dbSNP: rs1057519785
rs1057519785
ALK
1.000 0.040 2 29222404 missense variant A/C snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2012 2012
dbSNP: rs6731759
rs6731759
ALK
1.000 2 29804123 intron variant A/G snv 0.42
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 1 2019 2019
dbSNP: rs113994087
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.700 1.000 1 2011 2011
dbSNP: rs113994088
rs113994088
ALK
0.925 0.080 2 29222584 missense variant C/G snv
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.700 1.000 1 2011 2011
dbSNP: rs113994089
rs113994089
ALK
0.925 0.120 2 29220776 missense variant C/G;T snv
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.700 1.000 1 2011 2011
dbSNP: rs187926838
rs187926838
ALK
1.000 0.120 2 29595425 intron variant A/G snv 6.4E-03
CUI: C2004491
Disease: Cicatrix
Cicatrix
0.700 1.000 1 2019 2019
dbSNP: rs80270335
rs80270335
ALK
1.000 0.040 2 29393789 intron variant C/T snv 6.5E-02
CUI: C0011334
Disease: Dental caries
Dental caries
0.700 1.000 1 2019 2019
dbSNP: rs1406230
rs1406230
ALK
0.925 0.160 2 29360455 intron variant C/T snv 0.30
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2019 2019
dbSNP: rs187926838
rs187926838
ALK
1.000 0.120 2 29595425 intron variant A/G snv 6.4E-03
CUI: C3541994
Disease: Drug Hypersensitivity Syndrome
Drug Hypersensitivity Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs11903143
rs11903143
ALK
2 29369594 intron variant A/G snv 0.28
Granulocyte Colony Stimulating Factor Measurement
0.700 1.000 1 2017 2017
dbSNP: rs6731759
rs6731759
ALK
1.000 2 29804123 intron variant A/G snv 0.42
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 1 2019 2019
dbSNP: rs6731759
rs6731759
ALK
1.000 2 29804123 intron variant A/G snv 0.42
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 1 2019 2019
dbSNP: rs1406230
rs1406230
ALK
0.925 0.160 2 29360455 intron variant C/T snv 0.30
CUI: C0339471
Disease: Maculopathy with diabetes mellitus
Maculopathy with diabetes mellitus
0.700 1.000 1 2019 2019
dbSNP: rs113994087
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs113994087
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO
0.700 1.000 6 2008 2016
dbSNP: rs281864719
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO
0.700 1.000 6 1990 2016
dbSNP: rs863225281
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO
0.700 1.000 6 2008 2016
dbSNP: rs1057519697
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO
0.700 1.000 4 2008 2016
dbSNP: rs1057519698
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
NEUROBLASTOMA, SUSCEPTIBILITY TO
0.700 1.000 3 2008 2011