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: rs11187938
rs11187938
2 10 94423594 intron variant T/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs67183237
rs67183237
2 10 94486139 intron variant C/T snv 0.700 1.000 1 2017 2017