Source: ALL
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: rs10920573
rs10920573
ADORA1
1 1.000 0.080 1 203139380 intron variant T/C snv 0.51 0.010 1.000 1 2010 2010
dbSNP: rs17511192
rs17511192
ADORA1
1 1.000 0.080 1 203150363 intron variant C/T snv 0.32 0.010 1.000 1 2010 2010
dbSNP: rs3766553
rs3766553
ADORA1
1 1.000 0.080 1 203163914 intron variant A/G snv 0.51 0.010 1.000 1 2010 2010
dbSNP: rs3791878
rs3791878
GAD1
2 0.925 0.120 2 170815681 non coding transcript exon variant G/T snv 0.23 0.010 1.000 1 2013 2013
dbSNP: rs3828275
rs3828275
GAD1
1 1.000 0.080 2 170826230 intron variant C/T snv 0.36 0.010 1.000 1 2013 2013
dbSNP: rs4869682
rs4869682
SLC1A3
2 1.000 0.080 5 36656616 intron variant T/G snv 0.50 0.010 1.000 1 2019 2019
dbSNP: rs769391
rs769391
GAD1
1 1.000 0.080 2 170852920 non coding transcript exon variant A/G snv 0.29 0.010 1.000 1 2013 2013