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: rs3102735
rs3102735
TNFRSF11B ; COLEC10
12 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 1.000 1 2017 2017
dbSNP: rs12475342
rs12475342
SPTBN1
1 2 54655541 intron variant G/A snv 0.28 0.010 1.000 1 2012 2012
dbSNP: rs7570532
rs7570532
MSTN ; C2orf88
1 2 190058686 intron variant A/G snv 0.34 0.010 1.000 1 2013 2013
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2012 2012
dbSNP: rs1643821
rs1643821
ESR1
2 6 151862416 intron variant G/A snv 0.46 0.010 1.000 1 2012 2012
dbSNP: rs2234693
rs2234693
ESR1
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2012 2012
dbSNP: rs3087456
rs3087456
CIITA ; LOC105371080
14 0.742 0.480 16 10877045 intron variant G/A snv 0.53 0.010 1.000 1 2012 2012
dbSNP: rs1107748
rs1107748
LINC02594
3 1.000 0.080 17 43696446 intron variant T/C snv 0.54 0.010 1.000 1 2010 2010
dbSNP: rs1800544
rs1800544
ADRA2A
12 0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 0.010 1.000 1 2018 2018
dbSNP: rs2073618
rs2073618
TNFRSF11B ; COLEC10
19 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 0.020 1.000 2 2008 2017
dbSNP: rs2941584
rs2941584
SPTBN1
1 2 54654484 intron variant T/C snv 0.64 0.010 1.000 1 2012 2012
dbSNP: rs10085588
rs10085588
SEM1 ; LOC105375411 ; LOC105375412
3 1.000 0.080 7 96508362 intron variant A/G snv 0.72 0.010 1.000 1 2019 2019
dbSNP: rs4342521
rs4342521
SEM1 ; LOC105375411
2 7 96506693 missense variant T/G snv 0.72 0.010 1.000 1 2019 2019
dbSNP: rs11898505
rs11898505
SPTBN1
2 2 54457420 intron variant A/G snv 0.76 0.020 1.000 2 2010 2013
dbSNP: rs898604
rs898604
LRP4
1 11 46896432 intron variant G/A snv 0.76 0.010 1.000 1 2012 2012