rs1057519201, GABRB3

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, CHILDHOOD ABSENCE, 1
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
5 1.000 15 26621395 missense variant T/C snv 0.700 1.000 1 2017 2017
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
CUI: C2677087
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5
6 1.000 15 26621395 missense variant T/C snv 0.700 1.000 1 2017 2017