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: rs10752262
rs10752262
3 1.000 0.040 10 12353101 intron variant C/T snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs11257952
rs11257952
1 10 12714714 intron variant A/C snv 0.36 0.700 1.000 1 2018 2018