Source: ALL

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: rs525410
rs525410
1.000 0.080 1 183207295 intron variant A/G snv 0.47
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.800 1.000 1 2011 2011
dbSNP: rs80356683
rs80356683
1.000 0.080 1 183215467 stop gained C/T snv 4.0E-06
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 5 1994 2008
dbSNP: rs118203901
rs118203901
0.925 0.080 1 183222181 stop gained C/T snv 2.1E-05
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 2 2002 2006
dbSNP: rs2276543
rs2276543
1 183186170 upstream gene variant G/A snv 0.27
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 2 2018 2018
dbSNP: rs1057516473
rs1057516473
1.000 0.080 1 183243172 frameshift variant G/- delins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2006 2006
dbSNP: rs118203899
rs118203899
1.000 0.080 1 183225719 stop gained C/G;T snv
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 1994 1994
dbSNP: rs1217053724
rs1217053724
0.925 0.080 1 183243272 stop gained C/T snv 7.0E-06
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2017 2017
dbSNP: rs1217053724
rs1217053724
0.925 0.080 1 183243272 stop gained C/T snv 7.0E-06
Adult junctional epidermolysis bullosa (disorder)
0.700 1.000 1 2017 2017
dbSNP: rs151190720
rs151190720
1.000 0.080 1 183236593 stop gained C/G;T snv 6.8E-05
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2001 2001
dbSNP: rs1553266871
rs1553266871
1.000 0.080 1 183231028 frameshift variant GC/- del
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2004 2004
dbSNP: rs1553267882
rs1553267882
1.000 0.080 1 183243192 frameshift variant GAAGCTTTCCCGAGCCAAGA/- delins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2001 2001
dbSNP: rs1553267885
rs1553267885
1.000 0.080 1 183243228 frameshift variant A/- delins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2001 2001
dbSNP: rs201307156
rs201307156
1.000 0.080 1 183243203 stop gained C/T snv 4.0E-06
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2001 2001
dbSNP: rs3768610
rs3768610
1 183195338 intron variant G/A snv 8.6E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs672059
rs672059
1 183193404 intron variant G/A snv 0.57
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.700 1.000 1 2017 2017
dbSNP: rs753268823
rs753268823
1.000 0.080 1 183222115 stop gained C/T snv 4.0E-06
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2004 2004
dbSNP: rs778012079
rs778012079
1.000 0.080 1 183232331 frameshift variant TTTCAGA/- delins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 1.000 1 2006 2006
dbSNP: rs1043996591
rs1043996591
1.000 0.080 1 183227698 splice donor variant G/T snv 4.0E-06 2.8E-05
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0
dbSNP: rs1057516218
rs1057516218
1.000 0.080 1 183223248 frameshift variant GG/- del
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0
dbSNP: rs1057516383
rs1057516383
1.000 0.080 1 183235662 frameshift variant CTGC/- delins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0
dbSNP: rs1057516410
rs1057516410
1.000 0.080 1 183218489 splice donor variant G/C snv
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0
dbSNP: rs1057516444
rs1057516444
1.000 0.080 1 183220880 stop gained -/AA ins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0
dbSNP: rs1057516487
rs1057516487
1.000 0.080 1 183232186 splice acceptor variant G/A snv
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0
dbSNP: rs1057516569
rs1057516569
1.000 0.080 1 183232298 frameshift variant AG/- delins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0
dbSNP: rs1057516727
rs1057516727
1.000 0.080 1 183236542 frameshift variant CA/- delins
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
0.700 0