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: rs10427255
rs10427255 		2 1.000 0.040 2 145367955 intergenic variant C/T snv 0.55 0.700 1.000 1 2010 2010
dbSNP: rs6903896
rs6903896
HCG27
1 6 31200252 non coding transcript exon variant G/A snv 4.5E-02 0.700 1.000 1 2010 2010