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: rs1003688
rs1003688
SCGN
2 6 25658944 intron variant G/A snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs1321247
rs1321247
SCGN
2 6 25662645 intron variant A/T snv 6.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs1321248
rs1321248
SCGN
2 6 25662575 intron variant T/C snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs2205936
rs2205936
SCGN
4 0.925 0.120 6 25685264 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2294346
rs2294346
SCGN
4 0.925 0.120 6 25689259 intron variant G/C;T snv 0.46; 8.8E-06 0.700 1.000 1 2009 2009
dbSNP: rs2328891
rs2328891
SCGN
2 6 25669441 intron variant G/A snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs2876691
rs2876691
SCGN
2 6 25669297 intron variant G/A snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs9348689
rs9348689
SCGN
2 6 25684425 intron variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs9467550
rs9467550
SCGN
2 6 25653173 intron variant A/G snv 7.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs9467556
rs9467556
SCGN
3 6 25663957 intron variant T/C snv 0.16 0.700 1.000 1 2009 2009