Gene: SCGN ×
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: rs75639901
rs75639901
SCGN
2 1.000 0.080 6 25667803 intron variant A/G snv 4.8E-02 0.700 1.000 1 2018 2018