Gene: HMGA2 ×
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: rs8756
rs8756
HMGA2
7 0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 0.700 1.000 6 2008 2019
dbSNP: rs1042725
rs1042725
HMGA2
7 0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 0.700 1.000 5 2007 2019
dbSNP: rs1351394
rs1351394
HMGA2
5 12 65958046 3 prime UTR variant T/C;G snv 0.700 1.000 3 2010 2019
dbSNP: rs7979673
rs7979673
HMGA2
2 12 65833477 intron variant C/A;T snv 0.700 1.000 2 2011 2019
dbSNP: rs12371967
rs12371967
HMGA2
1 12 65952934 3 prime UTR variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs17179670
rs17179670
HMGA2
1 12 65956032 3 prime UTR variant A/G snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs73121716
rs73121716
HMGA2
1 12 65924437 intron variant C/T snv 1.1E-02 0.700 1.000 1 2019 2019