Source: ALL
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: rs10060683
rs10060683 		1 1.000 0.160 5 92523322 intron variant T/C snv 0.19 0.700 1.000 1 2012 2012