rs371918069, GCM2

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.
HYPERPARATHYROIDISM 4
CUI: C4479229
Disease: HYPERPARATHYROIDISM 4
4 1.000 6 10874372 missense variant C/T snv 5.6E-05 5.6E-05 0.700 0
Adenoma
CUI: C0001430
Disease: Adenoma
103 1.000 6 10874372 missense variant C/T snv 5.6E-05 5.6E-05 0.010 1.000 1 2019 2019