rs774211, RBMS2

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 12 56527155 intron variant T/C snv 0.12 0.700 1.000 1 2019 2019
Finding of Mean Corpuscular Hemoglobin
1206 12 56527155 intron variant T/C snv 0.12 0.700 1.000 1 2019 2019
Glutamine measurement
CUI: C0302274
Disease: Glutamine measurement
5 12 56527155 intron variant T/C snv 0.12 0.700 1.000 1 2019 2019
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 12 56527155 intron variant T/C snv 0.12 0.700 1.000 1 2012 2012