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: rs10870273
rs10870273
STK32C
1 1.000 0.080 10 132232632 intron variant A/G snv 0.72 0.700 1.000 1 2019 2019