Gene: COLEC10 ×
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: rs6469804
rs6469804
COLEC10
2 8 119032590 intron variant G/A;C snv 0.800 1.000 3 2008 2009
dbSNP: rs10505348
rs10505348
COLEC10
1 8 118960457 intergenic variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs13262276
rs13262276
COLEC10
1 8 119021679 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs13264172
rs13264172
COLEC10
1 8 119000622 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs13264791
rs13264791
COLEC10
1 8 119000851 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs1586274
rs1586274
COLEC10
1 8 119014323 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1905779
rs1905779
COLEC10
1 8 119028926 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1905780
rs1905780
COLEC10
1 8 119029411 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2062376
rs2062376
COLEC10
1 8 118997770 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2220189
rs2220189
COLEC10
1 8 118995469 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2326193
rs2326193
COLEC10
1 8 119017470 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs4242592
rs4242592
COLEC10
1 8 118956736 upstream gene variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs6469794
rs6469794
COLEC10
1 8 119003860 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs6999476
rs6999476
COLEC10
1 8 119020020 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs7010043
rs7010043
COLEC10
1 8 118999092 intron variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7013203
rs7013203
COLEC10
1 8 119004920 intron variant A/C;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7813486
rs7813486
COLEC10
1 8 119020286 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs7822098
rs7822098
COLEC10
1 8 119007890 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7842942
rs7842942
COLEC10
1 8 118996348 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs1385499
rs1385499
COLEC10
1 8 118962469 regulatory region variant G/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs1564860
rs1564860
COLEC10
1 8 118963431 intergenic variant C/T snv 0.34 0.700 1.000 2 2009 2009
dbSNP: rs7839059
rs7839059
COLEC10
2 8 118964303 intergenic variant C/A snv 0.40 0.800 1.000 2 2009 2013
dbSNP: rs1485302
rs1485302
COLEC10
1 8 118963905 intergenic variant G/A snv 0.50 0.700 1.000 1 2009 2009
dbSNP: rs1485303
rs1485303
COLEC10
1 8 118964017 intergenic variant G/A snv 0.50 0.700 1.000 1 2009 2009
dbSNP: rs1485310
rs1485310
COLEC10
1 8 119039417 intron variant A/T snv 0.52 0.700 1.000 1 2009 2009