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: rs3000073
rs3000073
1 14 105263455 intron variant G/A snv 0.28 0.800 1.000 1 2011 2011
dbSNP: rs4555082
rs4555082
2 14 105292627 intron variant C/T snv 0.30 0.700 1.000 1 2016 2016