rs10437868, NAV3

N. diseases: 2
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 77508538 intron variant T/C snv 9.4E-02 0.700 1.000 1 2019 2019
Leucine measurement
CUI: C0428209
Disease: Leucine measurement
3 12 77508538 intron variant T/C snv 9.4E-02 0.700 1.000 1 2019 2019