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: rs11668319
rs11668319
3 19 19185066 intron variant A/G snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs7360000
rs7360000
3 19 19156039 intron variant C/T snv 0.18 0.700 1.000 1 2012 2012