rs10830963, MTNR1B

N. diseases: 27
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.
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 1 2012 2012