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: rs323922
rs323922
NPSR1 ; NPSR1-AS1
1 7 34709170 intron variant G/C snv 0.45 0.010 1.000 1 2009 2009
dbSNP: rs324377
rs324377
NPSR1 ; NPSR1-AS1
1 7 34716363 intron variant C/A snv 0.47 0.010 1.000 1 2009 2009