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: rs11620955
rs11620955
FNTB ; MAX ; CHURC1-FNTB
14 65024537 intron variant A/G snv 0.58
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
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: rs11627531
rs11627531
FNTB ; MAX ; CHURC1-FNTB
14 65021078 intron variant T/C snv 0.57
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs11628273
rs11628273
FNTB ; MAX ; CHURC1-FNTB ; MIR4706
14 65043160 intron variant C/T snv 0.57
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs12435835
rs12435835
FNTB ; MAX ; CHURC1-FNTB
14 65033191 intron variant T/G snv 0.57
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs2296322
rs2296322
FNTB ; MAX ; CHURC1-FNTB
14 65012230 non coding transcript exon variant T/G snv 0.13
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4466998
rs4466998
FNTB ; MAX ; CHURC1-FNTB
14 65008822 intron variant C/A;G snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4586342
rs4586342
FNTB ; MAX ; CHURC1-FNTB
14 65007157 intron variant G/A;C snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs4899159
rs4899159
FNTB ; MAX ; CHURC1-FNTB
14 65013877 intron variant A/G;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs7148590
rs7148590
FNTB ; MAX ; CHURC1-FNTB
14 65006478 intron variant G/A snv 0.57
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs7155454
rs7155454
FNTB ; MAX ; CHURC1-FNTB
14 65035521 intron variant G/A snv 0.61
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs7158239
rs7158239
FNTB ; MAX ; CHURC1-FNTB
14 65053898 intron variant G/A snv 0.50
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2018 2018
dbSNP: rs726668
rs726668
FNTB ; MAX ; CHURC1-FNTB
14 65029098 intron variant A/G;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs8006419
rs8006419
FNTB ; MAX ; CHURC1-FNTB
14 65034017 intron variant A/G snv 0.61
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012