rs79977247, TTR

N. diseases: 9
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.
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 0.776 0.200 18 31592975 missense variant T/C;G snv 0.810 1.000 23 1986 2014
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.776 0.200 18 31592975 missense variant T/C;G snv 0.030 1.000 3 1992 2012
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.776 0.200 18 31592975 missense variant T/C;G snv 0.020 0.500 2 2007 2014
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.776 0.200 18 31592975 missense variant T/C;G snv 0.010 1.000 1 2013 2013
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.776 0.200 18 31592975 missense variant T/C;G snv 0.010 1.000 1 2013 2013
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.776 0.200 18 31592975 missense variant T/C;G snv 0.010 1.000 1 2013 2013
Seizures
CUI: C0036572
Disease: Seizures
553 0.776 0.200 18 31592975 missense variant T/C;G snv 0.010 1.000 1 2007 2007
Senile cardiac amyloidosis
CUI: C0268407
Disease: Senile cardiac amyloidosis
19 0.776 0.200 18 31592975 missense variant T/C;G snv 0.010 1.000 1 2007 2007
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
5 0.776 0.200 18 31592975 missense variant T/C;G snv 0.700 0