Source: GWASCAT

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: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
14 65020976 intron variant T/C snv 0.36
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
14 65020976 intron variant T/C snv 0.36
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
14 65020976 intron variant T/C snv 0.36
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
14 65020976 intron variant T/C snv 0.36
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
14 65020976 intron variant T/C snv 0.36
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016