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: rs11038167
rs11038167
TSPAN18
1 1.000 0.040 11 44821583 intron variant A/C;G snv 0.840 0.750 4 2011 2017