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: rs761885185
rs761885185
3 0.882 0.120 3 189869329 missense variant C/T snv 4.0E-06 0.020 1.000 2 2004 2011
dbSNP: rs34201045
rs34201045
1 1.000 0.040 3 189789729 5 prime UTR variant -/AG;AGA;AGAG;AGG;AGGG ins 0.010 1.000 1 2008 2008