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: rs104894078
rs104894078
0.851 0.080 8 74360184 missense variant C/T snv 7.0E-06
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
0.720 1.000 0 2010 2015
dbSNP: rs104894075
rs104894075
0.851 0.080 8 74362940 stop gained C/G snv 4.0E-06 2.1E-05
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
0.700 0
dbSNP: rs104894075
rs104894075
0.851 0.080 8 74362940 stop gained C/G snv 4.0E-06 2.1E-05
Charcot-Marie-Tooth disease, Type 4A, axonal form
0.700 0
dbSNP: rs104894077
rs104894077
0.790 0.080 8 74361886 stop gained C/T snv 7.6E-05 1.5E-04
NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
0.700 0
dbSNP: rs104894077
rs104894077
0.790 0.080 8 74361886 stop gained C/T snv 7.6E-05 1.5E-04
Charcot-Marie-Tooth disease, Type 4A, axonal form
0.700 0
dbSNP: rs104894077
rs104894077
0.790 0.080 8 74361886 stop gained C/T snv 7.6E-05 1.5E-04
Charcot-Marie-Tooth Disease, Recessive Intermediate A
0.700 0
dbSNP: rs104894077
rs104894077
0.790 0.080 8 74361886 stop gained C/T snv 7.6E-05 1.5E-04
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4
0.700 0
dbSNP: rs104894077
rs104894077
0.790 0.080 8 74361886 stop gained C/T snv 7.6E-05 1.5E-04
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
0.700 0
dbSNP: rs104894078
rs104894078
0.851 0.080 8 74360184 missense variant C/T snv 7.0E-06
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4
0.700 0
dbSNP: rs104894079
rs104894079
0.925 0.080 8 74360295 missense variant A/C snv
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
0.700 0
dbSNP: rs104894080
rs104894080
0.790 0.120 8 74364005 missense variant C/T snv 3.2E-05 4.2E-05
Creatine phosphokinase serum increased
0.700 0
dbSNP: rs104894080
rs104894080
0.790 0.120 8 74364005 missense variant C/T snv 3.2E-05 4.2E-05
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
0.700 0
dbSNP: rs104894080
rs104894080
0.790 0.120 8 74364005 missense variant C/T snv 3.2E-05 4.2E-05
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy
0.700 0
dbSNP: rs104894080
rs104894080
0.790 0.120 8 74364005 missense variant C/T snv 3.2E-05 4.2E-05
Charcot-Marie-Tooth Disease, Recessive Intermediate A
0.700 0
dbSNP: rs104894080
rs104894080
0.790 0.120 8 74364005 missense variant C/T snv 3.2E-05 4.2E-05
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised
0.700 0
dbSNP: rs104894080
rs104894080
0.790 0.120 8 74364005 missense variant C/T snv 3.2E-05 4.2E-05
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy
0.700 0
dbSNP: rs104894080
rs104894080
0.790 0.120 8 74364005 missense variant C/T snv 3.2E-05 4.2E-05
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
0.700 0
dbSNP: rs1060500978
rs1060500978
1.000 0.080 8 74364073 frameshift variant G/- delins
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
0.700 0
dbSNP: rs1060500979
rs1060500979
1.000 0.080 8 74361976 frameshift variant A/- delins
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
0.700 0
dbSNP: rs1174933176
rs1174933176
1.000 0.080 8 74360185 missense variant G/A snv 4.0E-06
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
0.700 0
dbSNP: rs121908112
rs121908112
1.000 0.080 8 74350553 stop gained G/A snv
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
0.700 0
dbSNP: rs121908114
rs121908114
1.000 0.080 8 74363051 missense variant C/T snv 1.6E-05 1.5E-04
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
0.700 0
dbSNP: rs121908115
rs121908115
1.000 0.080 8 74364009 missense variant G/A;C snv 4.0E-06
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
0.700 0
dbSNP: rs1323153568
rs1323153568
1.000 0.080 8 74364219 missense variant G/A snv 4.0E-06 7.0E-06
Charcot-Marie-Tooth disease, Type 4A, axonal form
0.700 0
dbSNP: rs1476856429
rs1476856429
0.882 0.080 8 74364057 missense variant A/G snv 1.2E-05 7.0E-06
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
0.700 0