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 5 2009 2013
dbSNP: rs7776054
rs7776054
HBS1L
13 6 135097778 intron variant A/G snv 0.24 0.800 1.000 3 2009 2018
dbSNP: rs9399137
rs9399137
HBS1L
13 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.800 1.000 1 2013 2013
dbSNP: rs12664956
rs12664956
HBS1L
2 6 135063050 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs13220662
rs13220662
HBS1L
4 6 135074410 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs1331309
rs1331309
HBS1L
2 6 135085040 intron variant T/G snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs148394396
rs148394396
HBS1L
1 6 135022389 intron variant A/T snv 4.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs1547247
rs1547247
HBS1L
5 6 135069698 intron variant G/A snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs567333455
rs567333455
HBS1L
1 6 135094331 intron variant AAA/-;A;AA;AAAA;AAAAA;AAAAAA delins 0.700 1.000 1 2016 2016
dbSNP: rs6904897
rs6904897
HBS1L
3 6 135061842 intron variant T/G snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs9389268
rs9389268
HBS1L
6 1.000 0.080 6 135098493 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017