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: rs1485305
rs1485305
COLEC10
1 8 118998281 intron variant A/T snv 0.54 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
dbSNP: rs1485312
rs1485312
COLEC10
1 8 119031696 intron variant T/C snv 0.58 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: rs1905777
rs1905777
COLEC10
1 8 119009601 intron variant A/T snv 0.67 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: rs1905783
rs1905783
COLEC10
1 8 119002597 intron variant C/T snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs1905784
rs1905784
COLEC10
1 8 119002384 intron variant G/A snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs2062375
rs2062375
COLEC10
2 1.000 0.080 8 118965553 intergenic variant G/C snv 0.65 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: rs2073617
rs2073617
TNFRSF11B ; COLEC10
9 0.776 0.360 8 118952044 upstream gene variant G/A snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs2073618
rs2073618
TNFRSF11B ; COLEC10
19 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 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: rs4305930
rs4305930
COLEC10
1 8 119045782 intron variant C/T snv 0.68 0.700 1.000 1 2009 2009
dbSNP: rs4307369
rs4307369
COLEC10
1 8 119024714 intron variant A/G snv 0.66 0.700 1.000 1 2009 2009
dbSNP: rs4335155
rs4335155
COLEC10
1 8 119001230 intron variant A/C snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs4354338
rs4354338
COLEC10
1 8 119003821 intron variant A/C snv 0.65 0.700 1.000 1 2009 2009
dbSNP: rs4401893
rs4401893
COLEC10
1 8 119032144 intron variant C/T snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs4403440
rs4403440
COLEC10
1 8 119019336 intron variant G/A snv 0.53 0.700 1.000 1 2009 2009
dbSNP: rs4424291
rs4424291
COLEC10
1 8 119006496 intron variant A/G snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs4495460
rs4495460
COLEC10
1 8 119007077 intron variant A/T snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs4563920
rs4563920
COLEC10
1 8 118981450 downstream gene variant A/G snv 0.61 0.700 1.000 1 2009 2009