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: rs13161895
rs13161895
2 1.000 0.040 5 180044201 intron variant C/T snv 0.12 0.700 1.000 1 2011 2011