rs137852779, EFHC1

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.
EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1
CUI: C2750892
Disease: EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1
2 1.000 0.040 6 52438538 missense variant A/G snv 4.0E-06 0.700 0
Epilepsy, Temporal Lobe
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
33 1.000 0.040 6 52438538 missense variant A/G snv 4.0E-06 0.010 1.000 1 2006 2006