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: rs2287623
rs2287623
1 2 168973645 intron variant G/A snv 0.57 0.800 1.000 1 2013 2018
dbSNP: rs11568373
rs11568373
3 2 168944893 synonymous variant T/C snv 5.8E-03 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs16856314
rs16856314
3 2 168966582 intron variant G/A snv 3.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs6709971
rs6709971
3 2 169011063 intron variant T/C snv 2.6E-02 0.700 1.000 1 2012 2012