rs7005606, NRG1

N. diseases: 3
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.
Congenital Intestinal Aganglionosis
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
16 0.925 0.080 8 32543983 intron variant T/G snv 0.39 0.700 1.000 2 2014 2016
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.925 0.080 8 32543983 intron variant T/G snv 0.39 0.700 1.000 2 2014 2016
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.925 0.080 8 32543983 intron variant T/G snv 0.39 0.700 1.000 1 2019 2019