SNCA, synuclein alpha, 6622

N. diseases: 449; N. variants: 66
Disease: Parkinson Disease ×
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: rs1372519
rs1372519 		1.000 0.040 4 89836158 5 prime UTR variant A/G snv 0.77
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1372520
rs1372520 		1.000 0.040 4 89836354 intron variant T/C snv 0.78
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs168552
rs168552 		1.000 0.040 4 89721993 intron variant C/T snv 0.80
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2298728
rs2298728 		1.000 0.040 4 89821664 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2572323
rs2572323 		1.000 0.040 4 89713401 intron variant A/G snv 0.75
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs356169
rs356169 		1.000 0.040 4 89711617 intron variant G/T snv 0.72
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs356174
rs356174 		1.000 0.040 4 89709750 intron variant G/T snv 0.72
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs356180
rs356180 		1.000 0.040 4 89706976 intron variant A/G snv 0.77
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs356200
rs356200 		0.882 0.160 4 89747463 intron variant T/C snv 0.44
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3775423
rs3775423 		1.000 0.040 4 89736340 intron variant C/T snv 0.24
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3775442
rs3775442 		1.000 0.040 4 89794080 intron variant C/T snv 6.7E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3857053
rs3857053 		1.000 0.040 4 89724523 3 prime UTR variant C/T snv 0.24
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs10014396
rs10014396 		1.000 0.040 4 89791478 intron variant T/C snv 0.17
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs356188
rs356188 		1.000 0.040 4 89770386 intron variant T/C snv 0.21
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs3796661
rs3796661 		1.000 0.040 4 89766356 intron variant C/T snv 8.7E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs201106962
rs201106962 		0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.090 1.000 9 2013 2019
dbSNP: rs431905511
rs431905511 		0.827 0.080 4 89828154 missense variant C/T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.070 1.000 7 2013 2020
dbSNP: rs2301134
rs2301134 		1.000 0.040 4 89837794 intron variant A/G snv 0.57
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2301135
rs2301135 		1.000 0.040 4 89837238 5 prime UTR variant G/C snv 0.58
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs356182
rs356182 		0.882 0.080 4 89704960 intron variant G/A snv 0.65
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.740 1.000 7 2014 2018
dbSNP: rs356186
rs356186 		1.000 0.040 4 89784213 intron variant A/G snv 0.80
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3775444
rs3775444 		1.000 0.040 4 89805385 intron variant C/T snv 6.7E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3756063
rs3756063 		0.925 0.080 4 89836243 intron variant G/C snv 0.58
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1330229174
rs1330229174 		0.925 0.080 4 89835568 missense variant T/C snv 4.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2017 2019
dbSNP: rs542171324
rs542171324 		0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2017 2018