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: rs16962767
rs16962767
1 16 56839877 3 prime UTR variant T/C snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs2241770
rs2241770
1 16 56832284 intron variant T/C snv 1.0E-01 9.7E-02 0.700 1.000 1 2009 2009