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: rs11984041
rs11984041
2 0.925 0.080 7 18992312 intron variant C/T snv 0.13 0.830 1.000 1 2012 2015
dbSNP: rs17347800
rs17347800
1 7 18477656 intron variant G/A;T snv 0.700 1.000 1 2015 2015