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: rs2296316
rs2296316
FNTB ; MAX ; CHURC1-FNTB
14 65053528 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
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: rs4466998
rs4466998
FNTB ; MAX ; CHURC1-FNTB
14 65008822 intron variant C/A;G snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 1.000 1 2009 2009
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: rs4899159
rs4899159
FNTB ; MAX ; CHURC1-FNTB
14 65013877 intron variant A/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
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: rs726668
rs726668
FNTB ; MAX ; CHURC1-FNTB
14 65029098 intron variant A/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs8006570
rs8006570
RAB15 ; CHURC1-FNTB
14 64945992 3 prime UTR variant G/A snv 5.4E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8006570
rs8006570
RAB15 ; CHURC1-FNTB
14 64945992 3 prime UTR variant G/A snv 5.4E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8006570
rs8006570
RAB15 ; CHURC1-FNTB
14 64945992 3 prime UTR variant G/A snv 5.4E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8006570
rs8006570
RAB15 ; CHURC1-FNTB
14 64945992 3 prime UTR variant G/A snv 5.4E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		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: rs2898885
rs2898885
RAB15 ; CHURC1-FNTB
14 64954556 intron variant T/C snv 0.19
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs28886684
rs28886684
FNTB ; MAX ; CHURC1-FNTB
14 65056577 intron variant T/C snv 0.24
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2412065
rs2412065
GPX2 ; CHURC1 ; CHURC1-FNTB
14 64940939 intron variant C/G snv 0.27
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2012 2012
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: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
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: 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: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
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: rs7148590
rs7148590
FNTB ; MAX ; CHURC1-FNTB
14 65006478 intron variant G/A snv 0.57
CUI: C1318315
Disease: Serum zinc measurement
Serum zinc measurement 		0.800 1.000 1 2013 2013
dbSNP: rs7148590
rs7148590
FNTB ; MAX ; CHURC1-FNTB
14 65006478 intron variant G/A snv 0.57
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
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