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: rs7996217
rs7996217
NALCN
1 1.000 0.160 13 101348594 intron variant T/G snv 1.6E-02 0.700 1.000 1 2012 2012