rs767543900, MAPT

N. diseases: 10
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.
Dementia
CUI: C0497327
Disease: Dementia
176 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2017 2017
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2004 2004
Forgetful
CUI: C0542476
Disease: Forgetful
18 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2019 2019
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1 2017 2017
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2019 2019
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2017 2017
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1 2017 2017
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1 2017 2017
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2017 2017
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 0.010 1.000 1 2004 2004