Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs74315371
rs74315371
SDHB
1 1.000 0.040 1 17028721 missense variant C/T snv 0.800 1.000 10 2001 2014