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: rs10103692
rs10103692 		2 0.925 0.080 8 54345567 intergenic variant A/G snv 0.13 0.010 1.000 1 2019 2019
dbSNP: rs10865710
rs10865710
PPARG
13 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs13266183
rs13266183 		2 0.925 0.080 8 54355052 non coding transcript exon variant C/T snv 0.22 0.010 1.000 1 2019 2019
dbSNP: rs2856830
rs2856830
HLA-DPA1
2 0.925 0.080 6 33073957 intron variant T/C snv 0.12 0.010 1.000 1 2019 2019