SPON1, spondin 1, 10418

N. diseases: 31; N. variants: 10
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11023139
rs11023139
1.000 0.080 11 14202800 intron variant G/A snv 6.5E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.800 1.000 1 2014 2014
dbSNP: rs10832169
rs10832169
11 14044939 intron variant G/A snv 0.39
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs11023056
rs11023056
11 14030572 intron variant A/G snv 0.48
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs117865811
rs117865811
11 14180763 intron variant A/G snv 6.3E-03
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement
0.700 1.000 1 2017 2017
dbSNP: rs117865811
rs117865811
11 14180763 intron variant A/G snv 6.3E-03
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement
0.700 1.000 1 2017 2017
dbSNP: rs17556665
rs17556665
11 14076935 intron variant G/T snv 7.4E-02
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1969539
rs1969539
11 14017074 intron variant A/G snv 0.48
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2303975
rs2303975
11 14255453 intron variant G/A snv 0.15
High density lipoprotein measurement
0.700 1.000 1 2017 2017
dbSNP: rs2618521
rs2618521
11 14031785 intron variant A/G snv 0.66
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs7102710
rs7102710
11 14244067 intron variant T/C snv 0.10
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs7102710
rs7102710
11 14244067 intron variant T/C snv 0.10
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
0.700 1.000 1 2017 2017
dbSNP: rs7102710
rs7102710
11 14244067 intron variant T/C snv 0.10
CUI: C0337437
Disease: Glucagon measurement
Glucagon measurement
0.700 1.000 1 2017 2017
dbSNP: rs2618516
rs2618516
0.882 0.080 11 14000092 intron variant T/C snv 0.65
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs2618516
rs2618516
0.882 0.080 11 14000092 intron variant T/C snv 0.65
CUI: C0497327
Disease: Dementia
Dementia
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs2618516
rs2618516
0.882 0.080 11 14000092 intron variant T/C snv 0.65
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018