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: rs437179
rs437179
3 0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 0.700 1.000 1 2014 2014
dbSNP: rs592229
rs592229
1 1.000 0.080 6 31962664 intron variant G/A;C;T snv 4.0E-06; 4.5E-05; 0.61 0.700 1.000 1 2014 2014