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: rs11766624
rs11766624
AUTS2
2 7 70422099 intron variant A/G snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs3804024
rs3804024
DSCAM ; DSCAM-IT1
2 21 40621781 intron variant T/C snv 9.0E-02 0.700 1.000 1 2012 2012