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: rs34881325
rs34881325
1 9 2622134 5 prime UTR variant C/T snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs7043199
rs7043199
2 1.000 0.040 9 2621145 intron variant T/A snv 0.18 0.700 1.000 1 2016 2016