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: rs10071838
rs10071838
LMBRD2 ; MIR580
5 36147704 intron variant C/A;T snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs10071838
rs10071838
LMBRD2 ; MIR580
5 36147704 intron variant C/A;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10941274
rs10941274
LMBRD2 ; MIR580
5 36147426 intron variant T/C snv 4.9E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs12655052
rs12655052
LMBRD2 ; MIR580
5 36149559 intron variant T/C snv 4.9E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013