rs12137595, None

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Charcot-Marie-Tooth Disease, Type Ia (disorder)
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
24 0.851 0.080 1 4034008 regulatory region variant C/T snv 8.6E-02 0.700 1.000 1 2019 2019
Hereditary and idiopathic neuropathy, unspecified
CUI: C0154754
Disease: Hereditary and idiopathic neuropathy, unspecified
6 0.851 0.080 1 4034008 regulatory region variant C/T snv 8.6E-02 0.700 1.000 1 2019 2019
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.851 0.080 1 4034008 regulatory region variant C/T snv 8.6E-02 0.700 1.000 1 2019 2019
NEUROPATHY, CONGENITAL HYPOMYELINATING, 2
CUI: C4722277
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 2
9 0.851 0.080 1 4034008 regulatory region variant C/T snv 8.6E-02 0.700 1.000 1 2019 2019
NEUROPATHY, CONGENITAL HYPOMYELINATING, 3
CUI: C4748608
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 3
13 0.851 0.080 1 4034008 regulatory region variant C/T snv 8.6E-02 0.700 1.000 1 2019 2019