Gene: SNCA ×
Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2197120
rs2197120
SNCA
1 1.000 0.040 4 89808451 intron variant A/G snv 0.78 0.700 1.000 2 2011 2012
dbSNP: rs181489
rs181489
SNCA ; LOC105377329
1 1.000 0.040 4 89713869 intron variant T/A;C snv 0.710 1.000 2 2011 2015
dbSNP: rs168552
rs168552
SNCA ; LOC105377329
1 1.000 0.040 4 89721993 intron variant C/T snv 0.80 0.700 1.000 1 2011 2011
dbSNP: rs1372520
rs1372520
SNCA ; SNCA-AS1
1 1.000 0.040 4 89836354 intron variant T/C snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs1372519
rs1372519
SNCA ; SNCA-AS1
1 1.000 0.040 4 89836158 5 prime UTR variant A/G snv 0.77 0.700 1.000 1 2011 2011
dbSNP: rs11931074
rs11931074
SNCA ; LOC105377329
1 0.851 0.080 4 89718364 intron variant G/A;C;T snv 0.900 1.000 4 2009 2020
dbSNP: rs10516845
rs10516845
SNCA
1 1.000 0.040 4 89763127 intron variant A/G;T snv 0.700 1.000 1 2011 2011