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: rs1876829
rs1876829
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1876829
rs1876829
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012