Gene: CLEC16A ×
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: rs11865121
rs11865121
CLEC16A
1 1.000 0.080 16 11072831 intron variant C/A snv 0.40 0.800 1.000 1 2009 2009
dbSNP: rs7200786
rs7200786
CLEC16A
3 0.882 0.200 16 11083944 intron variant A/G snv 0.59 0.800 1.000 1 2011 2011
dbSNP: rs12708716
rs12708716
CLEC16A
7 0.807 0.320 16 11086016 intron variant A/G snv 0.37 0.710 1.000 2 2011 2011
dbSNP: rs11860603
rs11860603
CLEC16A
1 1.000 0.080 16 11071160 intron variant T/C snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs12927355
rs12927355
CLEC16A
3 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs6498160
rs6498160
CLEC16A
1 1.000 0.080 16 11105590 intron variant T/C snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs6498168
rs6498168
CLEC16A
1 1.000 0.080 16 11141273 intron variant T/G snv 0.71 0.700 1.000 1 2016 2016
dbSNP: rs7184083
rs7184083
CLEC16A ; LOC105371081
1 1.000 0.080 16 11134057 intron variant A/G snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs6498169
rs6498169
CLEC16A
6 0.807 0.280 16 11155472 non coding transcript exon variant G/A snv 0.66 0.030 1.000 3 2009 2012
dbSNP: rs725613
rs725613
CLEC16A
4 0.851 0.240 16 11075826 intron variant T/G snv 0.42 0.020 1.000 2 2009 2011
dbSNP: rs1465201414
rs1465201414
CLEC16A
1 1.000 0.080 16 10971132 missense variant A/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs2041670
rs2041670
CLEC16A
4 0.851 0.280 16 11080795 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs2080272
rs2080272
CLEC16A
1 1.000 0.080 16 11117696 intron variant A/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs2903692
rs2903692
CLEC16A
6 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.010 1.000 1 2009 2009
dbSNP: rs8056098
rs8056098
CLEC16A
1 1.000 0.080 16 11044955 intron variant G/A;C;T snv 0.010 1.000 1 2020 2020
dbSNP: rs998592
rs998592
CLEC16A
2 0.925 0.160 16 11105821 intron variant C/T snv 0.39 0.010 1.000 1 2011 2011