Source: CURATED

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: rs1009977
rs1009977
LGALS3
1.000 0.040 14 55136284 intron variant T/G snv 0.48
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1009978
rs1009978
LGALS3
14 55136343 intron variant C/G;T snv
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10498475
rs10498475
LGALS3
14 55145762 downstream gene variant C/T snv 5.7E-02
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075601
rs2075601
LGALS3
14 55142516 intron variant C/T snv 0.57
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075602
rs2075602
LGALS3
14 55143056 intron variant A/G;T snv
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075603
rs2075603
LGALS3
14 55143237 intron variant C/A snv 0.36
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3825613
rs3825613
LGALS3
14 55126454 intron variant A/C snv 0.36
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4644
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4652
rs4652
LGALS3
0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs76426991
rs76426991
LGALS3
14 55134221 intron variant G/A snv 5.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8004787
rs8004787
LGALS3
14 55140648 intron variant C/T snv 0.57
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8013027
rs8013027
LGALS3
14 55144222 intron variant C/G snv 0.42
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012