Gene: SCGB3A2 ×
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: rs1368408
rs1368408
SCGB3A2 ; C5orf46
2 0.925 0.160 5 147878599 intron variant G/A snv 0.21 0.010 1.000 1 2017 2017
dbSNP: rs6882292
rs6882292
SCGB3A2 ; C5orf46
1 1.000 0.080 5 147877993 intron variant G/A snv 7.3E-02 0.010 1.000 1 2017 2017