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: rs356174
rs356174
SNCA ; LOC105377329
1 1.000 0.040 4 89709750 intron variant G/T snv 0.72 0.700 1.000 1 2011 2011
dbSNP: rs356180
rs356180
SNCA ; LOC105377329
1 1.000 0.040 4 89706976 intron variant A/G snv 0.77 0.700 1.000 1 2011 2011
dbSNP: rs356188
rs356188
SNCA
1 1.000 0.040 4 89770386 intron variant T/C snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs356200
rs356200
SNCA
1 0.882 0.160 4 89747463 intron variant T/C snv 0.44 0.700 1.000 1 2011 2011
dbSNP: rs3775423
rs3775423
SNCA
1 1.000 0.040 4 89736340 intron variant C/T snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs3796661
rs3796661
SNCA
1 1.000 0.040 4 89766356 intron variant C/T snv 8.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs3857053
rs3857053
SNCA
1 1.000 0.040 4 89724523 3 prime UTR variant C/T snv 0.24 0.700 1.000 1 2011 2011