rs267606697, CACNA1H

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.
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6
13 0.925 0.040 16 1204325 missense variant G/A snv 2.4E-04 4.2E-05 0.700 0
Absence Epilepsy
CUI: C0014553
Disease: Absence Epilepsy
17 0.925 0.040 16 1204325 missense variant G/A snv 2.4E-04 4.2E-05 0.010 1.000 1 2005 2005
Childhood Absence Epilepsy
CUI: C4281785
Disease: Childhood Absence Epilepsy
13 0.925 0.040 16 1204325 missense variant G/A snv 2.4E-04 4.2E-05 0.010 1.000 1 2005 2005