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: rs1179907
rs1179907
ANKRD6 ; LYRM2
6 89615130 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs16882001
rs16882001
ANKRD6 ; LYRM2
6 89612518 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4269347
rs4269347
ANKRD6 ; LYRM2
6 89587169 intron variant C/G;T snv
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs4707554
rs4707554
ANKRD6 ; LYRM2
6 89611690 intron variant C/T snv 0.67
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs4707554
rs4707554
ANKRD6 ; LYRM2
6 89611690 intron variant C/T snv 0.67
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: rs6905628
rs6905628
LYRM2
6 89635150 3 prime UTR variant C/G snv 0.73
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019