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: rs10228350
rs10228350
FOXP2
2 1.000 0.040 7 114420608 intron variant A/G;T snv 0.700 1.000 1 2019 2019