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: rs3817963
rs3817963
BTNL2 ; TSBP1-AS1
0.776 0.360 6 32400310 intron variant T/C snv 0.25
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2013 2013
dbSNP: rs2076530
rs2076530
BTNL2 ; TSBP1-AS1
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2007 2007
dbSNP: rs2076533
rs2076533
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32395750 intron variant C/T snv 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2007 2007
dbSNP: rs3763307
rs3763307
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32406845 non coding transcript exon variant A/T snv 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2007 2007
dbSNP: rs3806156
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2007 2007
dbSNP: rs9268480
rs9268480
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32396067 synonymous variant C/T snv 0.26 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2007 2007