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: rs2062377
rs2062377
COLEC10
2 8 118995181 upstream gene variant T/A snv 0.67 0.800 1.000 3 2009 2013
dbSNP: rs6469804
rs6469804
COLEC10
2 8 119032590 intron variant G/A;C snv 0.800 1.000 3 2008 2009
dbSNP: rs6993813
rs6993813
COLEC10
2 1.000 0.080 8 119039999 intron variant T/C snv 0.60 0.800 1.000 3 2008 2009
dbSNP: rs11995824
rs11995824
COLEC10
1 8 119000461 intron variant C/G snv 0.65 0.800 1.000 2 2009 2018
dbSNP: rs2450083
rs2450083
COLEC10
2 1.000 0.080 8 119051303 intron variant T/C snv 0.59 0.800 1.000 2 2009 2014
dbSNP: rs4424296
rs4424296
COLEC10
2 8 119001037 intron variant C/T snv 0.61 0.800 1.000 2 2009 2014
dbSNP: rs7839059
rs7839059
COLEC10
2 8 118964303 intergenic variant C/A snv 0.40 0.800 1.000 2 2009 2013
dbSNP: rs1564860
rs1564860
COLEC10
1 8 118963431 intergenic variant C/T snv 0.34 0.700 1.000 2 2009 2009
dbSNP: rs6469792
rs6469792
COLEC10
1 8 118996132 intron variant T/C snv 0.62 0.700 1.000 2 2009 2009
dbSNP: rs10086835
rs10086835
COLEC10
1 8 119027942 intron variant C/T snv 0.63 0.700 1.000 1 2009 2009
dbSNP: rs10091277
rs10091277
COLEC10
1 8 119022148 intron variant A/G snv 0.53 0.700 1.000 1 2009 2009
dbSNP: rs10098408
rs10098408
COLEC10
1 8 119027482 intron variant T/C snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs10505348
rs10505348
COLEC10
1 8 118960457 intergenic variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10505351
rs10505351
COLEC10
1 8 119021759 intron variant C/T snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs10955919
rs10955919
COLEC10
1 8 119008679 intron variant C/G snv 0.62 0.700 1.000 1 2009 2009
dbSNP: rs10955924
rs10955924
COLEC10
1 8 119041104 intron variant C/A snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs11992136
rs11992136
COLEC10
1 8 118991488 upstream gene variant C/G snv 0.61 0.700 1.000 1 2009 2009
dbSNP: rs12682278
rs12682278
COLEC10
1 8 119020089 intron variant A/G snv 0.68 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: rs1385499
rs1385499
COLEC10
1 8 118962469 regulatory region variant G/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs1485295
rs1485295
COLEC10
1 8 119027223 intron variant A/G snv 0.64 0.700 1.000 1 2009 2009
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