Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs71413877
rs71413877
LONRF2
2 100308360 intron variant G/A snv 2.6E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 3 2018 2019
dbSNP: rs10183150
rs10183150
LONRF2
2 100322655 upstream gene variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs11895772
rs11895772
LONRF2
2 100322455 5 prime UTR variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs4851284
rs4851284
LONRF2
2 100278425 3 prime UTR variant C/T snv 0.67
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs4851287
rs4851287
LONRF2
2 100299310 missense variant A/G snv 0.69 0.72
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs6542924
rs6542924
LONRF2
2 100276651 3 prime UTR variant C/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs71413877
rs71413877
LONRF2
2 100308360 intron variant G/A snv 2.6E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs75152355
rs75152355
LONRF2
2 100319907 intron variant T/C snv 1.4E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs7582180
rs7582180
LONRF2
2 100296001 intron variant A/G snv 0.72
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs7606277
rs7606277
LONRF2
2 100313064 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs773205136
rs773205136
LONRF2
1.000 0.080 2 100294302 missense variant G/A snv 4.1E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 0