Gene: BTNL2 ×
Source: GWASDB ×
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: rs1980493
rs1980493
BTNL2 ; TSBP1-AS1
6 0.776 0.400 6 32395438 intron variant T/C snv 0.13 0.800 1.000 1 2007 2015
dbSNP: rs2076530
rs2076530
BTNL2 ; TSBP1-AS1
5 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 0.710 1.000 1 2005 2007
dbSNP: rs3763313
rs3763313
BTNL2
5 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2007 2007
dbSNP: rs3793126
rs3793126
BTNL2 ; TSBP1-AS1
3 0.882 0.240 6 32403842 intron variant A/G snv 0.24 0.700 1.000 1 2007 2007
dbSNP: rs3806156
rs3806156
BTNL2 ; TSBP1-AS1
5 0.827 0.280 6 32405921 intron variant G/A;T snv 0.700 1.000 1 2007 2007
dbSNP: rs3817963
rs3817963
BTNL2 ; TSBP1-AS1
5 0.776 0.360 6 32400310 intron variant T/C snv 0.25 0.700 1.000 1 2007 2007
dbSNP: rs3817973
rs3817973
BTNL2 ; HCG23 ; TSBP1-AS1
2 0.925 0.200 6 32393334 intron variant C/T snv 0.39 0.700 1.000 1 2007 2007