Gene: HBS1L ×
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: rs7776054
rs7776054
HBS1L
13 6 135097778 intron variant A/G snv 0.24 0.800 1.000 4 2012 2018
dbSNP: rs7775698
rs7775698
HBS1L
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 3 2010 2012
dbSNP: rs4896131
rs4896131
HBS1L
1 6 135070962 intron variant C/A snv 0.56 0.700 1.000 2 2016 2018
dbSNP: rs9373124
rs9373124
HBS1L
3 6 135102071 intron variant T/C snv 0.33 0.800 1.000 2 2009 2012
dbSNP: rs9376090
rs9376090
HBS1L
7 6 135090090 intron variant T/C snv 0.19 0.800 1.000 2 2012 2017
dbSNP: rs1014021
rs1014021
HBS1L
1 6 135013462 intron variant A/G snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs1041480
rs1041480
HBS1L
1 6 135051938 intron variant G/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs10484496
rs10484496
HBS1L
1 6 134978544 intron variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs1074849
rs1074849
HBS1L
2 6 135102274 intron variant G/A snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs10872427
rs10872427
HBS1L
1 6 135032314 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs11154791
rs11154791
HBS1L
1 6 135058010 intron variant A/G snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs1135205
rs1135205
HBS1L
1 6 134960657 3 prime UTR variant C/T snv 0.53 0.700 1.000 1 2012 2012
dbSNP: rs11752907
rs11752907
HBS1L
1 6 135070357 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11754021
rs11754021
HBS1L
1 6 134987237 intron variant A/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs11755229
rs11755229
HBS1L
1 6 135048775 intron variant A/G snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs11756988
rs11756988
HBS1L
1 6 135026457 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs11757577
rs11757577
HBS1L
2 6 135070327 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11758774
rs11758774
HBS1L
1 6 135062651 intron variant T/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs11759062
rs11759062
HBS1L
1 6 135060110 intron variant A/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs11759077
rs11759077
HBS1L
1 6 135060213 splice acceptor variant A/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs11759553
rs11759553
HBS1L
2 6 135101158 intron variant A/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs12526055
rs12526055
HBS1L
1 6 135004780 intron variant C/T snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs12661423
rs12661423
HBS1L
1 6 135028432 intron variant C/T snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs12663447
rs12663447
HBS1L
1 6 134995888 intron variant A/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs12663810
rs12663810
HBS1L
1 6 134968644 intron variant G/A;C snv 0.700 1.000 1 2012 2012