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: rs10491487
rs10491487
RASGRF2
1.000 0.120 5 81027549 intron variant T/G snv 8.2E-02
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular 		0.700 1.000 1 2012 2012
dbSNP: rs26906
rs26906
RASGRF2
1.000 0.120 5 81069068 intron variant T/C snv 0.86
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular 		0.700 1.000 1 2012 2012