Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11865121
rs11865121
CLEC16A
1.000 0.080 16 11072831 intron variant C/A snv 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2009 2009
dbSNP: rs7200786
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs12708716
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.710 1.000 1 2011 2011
dbSNP: rs11860603
rs11860603
CLEC16A
1.000 0.080 16 11071160 intron variant T/C snv 0.41
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2009 2009
dbSNP: rs7184083
rs7184083
CLEC16A ; LOC105371081
1.000 0.080 16 11134057 intron variant A/G snv 0.72
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2009 2009