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: rs76481776
rs76481776
MIR182 ; LOC105375501
4 0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02 0.010 1.000 1 2010 2010
dbSNP: rs33458
rs33458
LYZL4
2 1.000 0.040 3 42362535 intergenic variant C/A;G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs4822492
rs4822492
ADORA2A-AS1
4 1.000 0.040 22 24447626 intron variant C/G snv 0.47 0.010 1.000 1 2019 2019
dbSNP: rs619002
rs619002
EHD3
2 1.000 0.040 2 31266099 intron variant C/T snv 0.86 0.010 1.000 1 2012 2012
dbSNP: rs644926
rs644926
EHD3
2 1.000 0.040 2 31266861 3 prime UTR variant T/C snv 0.86 0.010 1.000 1 2012 2012