Source: ALL
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: rs10136383
rs10136383 		2 0.925 0.040 14 22332649 intron variant C/T snv 6.4E-02 0.700 1.000 1 2018 2018