Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9468304
rs9468304
ELOVL2 ; ELOVL2-AS1
1.000 0.040 6 11041932 intron variant G/A snv 0.19
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs9468304
rs9468304
ELOVL2 ; ELOVL2-AS1
1.000 0.040 6 11041932 intron variant G/A snv 0.19
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.010 1.000 1 2018 2018