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: rs1131690935
rs1131690935
19 1221973 inframe deletion GGTTCTCCATCCGGCAGA/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 7 1992 2014
dbSNP: rs1131690916
rs1131690916
19 1207059 inframe deletion ATGGGGGACCTG/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2009 2013
dbSNP: rs1057518830
rs1057518830
1.000 0.040 19 1221331 inframe deletion CTG/- delins
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation
0.700 0
dbSNP: rs1057518830
rs1057518830
1.000 0.040 19 1221331 inframe deletion CTG/- delins
CUI: C1257915
Disease: Intestinal Polyposis
Intestinal Polyposis
0.700 0
dbSNP: rs1131690953
rs1131690953
19 1207065 inframe deletion CCTGCTGGGGGA/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs587776660
rs587776660
1.000 0.160 19 1221994 inframe deletion TCCGGCAGC/- del
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 0
dbSNP: rs730881958
rs730881958
19 1207047 inframe deletion TCATCGGCAAGT/- del
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs876658584
rs876658584
1.000 0.160 19 1218415 splice acceptor variant A/G snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 4 1999 2013
dbSNP: rs112675807
rs112675807
1.000 0.160 19 1218416 splice acceptor variant G/A;C;T snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 3 2000 2005
dbSNP: rs1131690934
rs1131690934
19 1220579 splice acceptor variant A/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 2 2001 2006
dbSNP: rs1555738319
rs1555738319
1.000 0.160 19 1220580 splice acceptor variant G/A snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 2 2004 2005
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: rs1057517830
rs1057517830
19 1221212 splice acceptor variant G/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs1131690944
rs1131690944
19 1221947 splice acceptor variant A/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs398123406
rs398123406
19 1222984 splice acceptor variant G/C;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs587776658
rs587776658
1.000 0.160 19 1220372 splice acceptor variant G/A snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 0
dbSNP: rs727504172
rs727504172
1.000 0.160 19 1222983 splice acceptor variant A/C;T snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 0
dbSNP: rs863224448
rs863224448
1.000 0.160 19 1221948 splice acceptor variant G/A snv
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 0
dbSNP: rs876658584
rs876658584
1.000 0.160 19 1218415 splice acceptor variant A/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs121913321
rs121913321
1.000 0.160 19 1221315 frameshift variant CC/-;C;CCC delins
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 5 1998 2010
dbSNP: rs397518440
rs397518440
1.000 0.160 19 1219367 frameshift variant C/- del
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 4 1998 2007
dbSNP: rs1131690917
rs1131690917
1.000 0.160 19 1207066 frameshift variant GGG/-;G;GGGG delins
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 3 1999 2013
dbSNP: rs121913321
rs121913321
1.000 0.160 19 1221315 frameshift variant CC/-;C;CCC delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 3 2005 2005
dbSNP: rs786205864
rs786205864
1.000 0.160 19 1221321 frameshift variant -/C delins
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 3 2000 2005
dbSNP: rs121913320
rs121913320
1.000 0.160 19 1221265 frameshift variant TTTG/- delins
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
0.700 1.000 2 1998 2005