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: rs55730005
rs55730005
UNC119B
12 120719733 intron variant C/A;G snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 2 2017 2019
dbSNP: rs55730005
rs55730005
UNC119B
12 120719733 intron variant C/A;G snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 2 2017 2019
dbSNP: rs17847
rs17847
UNC119B
12 120711672 non coding transcript exon variant A/G snv 0.60
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs2066938
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2011 2011
dbSNP: rs2066938
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2066938
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2011 2011
dbSNP: rs34734847
rs34734847
UNC119B
12 120716418 intron variant T/C snv 0.38
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs3833788
rs3833788
UNC119B
12 120713260 splice acceptor variant CTCTTGT/-;CTCTTGTCTCTTGT delins 0.37
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs556001
rs556001
UNC119B
12 120715164 intron variant A/G snv 0.45
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs56273049
rs56273049
UNC119B
12 120718238 intron variant A/T snv 0.38
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs696337
rs696337
UNC119B ; MIR4700
12 120721577 3 prime UTR variant T/C snv 0.60
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012