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: rs11078936
rs11078936
1 1.000 0.080 17 40041661 intron variant T/C snv 0.29 0.700 1.000 1 2010 2010
dbSNP: rs9916158
rs9916158
1 1.000 0.080 17 40025976 intron variant G/T snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs2302777
rs2302777
2 0.925 0.200 17 40023239 synonymous variant A/G snv 0.39 0.30 0.010 1.000 1 2016 2016