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: rs11095197
rs11095197
1 1.000 0.040 X 30958830 intron variant C/T snv 0.28 0.700 1.000 1 2011 2011