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: rs11575937
rs11575937
29 0.653 0.480 1 156136985 missense variant G/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs397517892
rs397517892
4 0.851 0.240 1 156136419 missense variant C/T snv 9.9E-06 1.4E-05 0.010 1.000 1 2009 2009