Source: CLINVAR

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: rs1057519858
rs1057519858
1.000 0.080 19 1220495 missense variant G/T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.700 1.000 1 2014 2014
dbSNP: rs1057520017
rs1057520017
1.000 0.040 19 1220630 missense variant C/T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2007 2007
dbSNP: rs1057520038
rs1057520038
0.925 0.160 19 1220627 missense variant G/A snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 1 2011 2011
dbSNP: rs1057520039
rs1057520039
0.882 0.200 19 1207169 stop gained C/G;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2007 2007
dbSNP: rs1057520040
rs1057520040
1.000 0.160 19 1218449 missense variant A/G snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 1 1999 1999
dbSNP: rs1131690917
rs1131690917
1.000 0.160 19 1207066 frameshift variant GGG/-;G;GGGG delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2001 2001
dbSNP: rs1131690931
rs1131690931
19 1220371 splice acceptor variant A/C snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2001 2001
dbSNP: rs1131690947
rs1131690947
19 1221962 frameshift variant C/- del
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2010 2010
dbSNP: rs121913315
rs121913315
0.882 0.160 19 1220488 missense variant G/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913315
rs121913315
0.882 0.160 19 1220488 missense variant G/A;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2007 2007
dbSNP: rs121913316
rs121913316
1.000 0.080 19 1220489 missense variant A/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913317
rs121913317
1.000 0.080 19 1220503 stop gained G/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913319
rs121913319
19 1207078 frameshift variant G/-;GG delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 1998 1998
dbSNP: rs121913320
rs121913320
1.000 0.160 19 1221265 frameshift variant TTTG/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 1998 1998
dbSNP: rs121913322
rs121913322
0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913323
rs121913323
1.000 0.040 19 1220416 stop gained C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913324
rs121913324
1.000 0.160 19 1207022 stop gained C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs121913325
rs121913325
19 1223060 stop gained G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs137853079
rs137853079
1.000 0.120 19 1207021 stop gained C/A;G;T snv 1.6E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2014 2014
dbSNP: rs1555737814
rs1555737814
1.000 0.160 19 1219389 frameshift variant GT/- del
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 1 2017 2017
dbSNP: rs1555738683
rs1555738683
1.000 0.160 19 1221299 frameshift variant T/AC delins
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 1 2006 2006
dbSNP: rs587778695
rs587778695
1.000 0.160 19 1223152 missense variant C/A;T snv 4.1E-06; 8.2E-05
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 1 2012 2012
dbSNP: rs587782424
rs587782424
1.000 0.160 19 1219346 frameshift variant TG/- delins
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 1 2010 2010
dbSNP: rs730881970
rs730881970
19 1219358 stop gained C/A;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2004 2004
dbSNP: rs730881972
rs730881972
1.000 0.080 19 1220395 missense variant G/C;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2007 2007