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: rs6428370
rs6428370 		1 1.000 0.040 1 196875463 intron variant A/C;G snv 0.38 0.700 1.000 2 2013 2013