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: rs16971217
rs16971217
1 17 35617036 intron variant C/A;G snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs112346425
rs112346425
1 17 35680792 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11868206
rs11868206
1 17 35632228 intron variant G/A snv 0.23 0.700 1.000 1 2016 2016