Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7652177
rs7652177
3 172251287 missense variant C/G snv 0.54 0.61
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 4 2010 2019
dbSNP: rs4243400
rs4243400
3 172253069 intron variant A/G snv 0.60
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 2 2015 2019
dbSNP: rs11718418
rs11718418
3 172053964 intron variant A/G snv 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs4535251
rs4535251
3 172208583 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2013 2013
dbSNP: rs4894539
rs4894539
3 172281493 intron variant G/T snv 0.53
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs4894797
rs4894797
3 172065756 intron variant G/A snv 0.47
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs62281815
rs62281815
3 172252520 intron variant A/T snv 0.41
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017