Source: GWASDB

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: rs12220534
rs12220534
RASGEF1A
1.000 0.080 10 43238858 intron variant T/G snv 0.16
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 1.000 1 2009 2009
dbSNP: rs1879310
rs1879310
RASGEF1A
1.000 0.080 10 43239327 intron variant T/C snv 0.16
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 1.000 1 2009 2009
dbSNP: rs28461806
rs28461806
RASGEF1A
10 43260306 intron variant T/C snv 1.7E-05
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs7090455
rs7090455
RASGEF1A
1.000 0.080 10 43258084 intron variant C/T snv 0.13
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 1.000 1 2009 2009
dbSNP: rs7093409
rs7093409
RASGEF1A
1.000 0.080 10 43244619 intron variant A/G snv 0.18
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 1.000 1 2009 2009