rs10986018, GABBR2

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.
Homocysteine measurement
CUI: C2242817
Disease: Homocysteine measurement
33 9 98361054 intron variant T/C snv 7.9E-02 0.700 1.000 1 2009 2009
VITAMIN B12 MEASUREMENT
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
22 9 98361054 intron variant T/C snv 7.9E-02 0.700 1.000 1 2009 2009