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: rs57045855
rs57045855
6 0.882 0.040 1 156134464 missense variant A/G;T snv 0.010 1.000 1 2006 2006
dbSNP: rs61195471
rs61195471
6 0.827 0.160 1 156134496 missense variant G/A snv 0.010 1.000 1 2001 2001
dbSNP: rs61661343
rs61661343
4 0.851 0.040 1 156130687 missense variant T/C snv 0.010 1.000 1 2004 2004