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: rs7775698
rs7775698
HBS1L
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 4 2009 2012
dbSNP: rs1547247
rs1547247
HBS1L
5 6 135069698 intron variant G/A snv 0.22 0.800 1.000 3 2009 2019
dbSNP: rs9376090
rs9376090
HBS1L
7 6 135090090 intron variant T/C snv 0.19 0.800 1.000 2 2009 2018
dbSNP: rs1074849
rs1074849
HBS1L
2 6 135102274 intron variant G/A snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs11759553
rs11759553
HBS1L
2 6 135101158 intron variant A/T snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs13192235
rs13192235
HBS1L
2 6 135025213 intron variant G/A snv 4.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs13220662
rs13220662
HBS1L
4 6 135074410 intron variant G/A snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs2210366
rs2210366
HBS1L
4 6 135094070 intron variant G/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs34164109
rs34164109
HBS1L
2 6 135100038 intron variant C/T snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs35367489
rs35367489
HBS1L
1 6 135023317 intron variant G/A snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs41294858
rs41294858
HBS1L
1 6 135091498 intron variant T/C snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs7776054
rs7776054
HBS1L
13 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs9373124
rs9373124
HBS1L
3 6 135102071 intron variant T/C snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs9389266
rs9389266
HBS1L
2 6 135090599 intron variant G/T snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs9389268
rs9389268
HBS1L
6 1.000 0.080 6 135098493 intron variant A/G snv 0.24 0.700 1.000 1 2009 2009
dbSNP: rs9399135
rs9399135
HBS1L
2 6 135047176 intron variant G/A snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs9399137
rs9399137
HBS1L
13 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs9483783
rs9483783
HBS1L
2 6 135079902 intron variant T/C snv 2.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs9494139
rs9494139
HBS1L
2 6 135093655 intron variant A/G snv 0.15 0.700 1.000 1 2009 2009