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: rs1801133
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0.800 1.000 3 2009 2018
dbSNP: rs17375901
rs17375901
MTHFR
1.000 0.080 1 11792459 intron variant C/T snv 4.6E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.800 1.000 1 2009 2009
dbSNP: rs1801133
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.760 1.000 1 2008 2017
dbSNP: rs17367504
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 2 2009 2011
dbSNP: rs17367504
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs13306560
rs13306560
CLCN6 ; MTHFR
1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2010 2010
dbSNP: rs1476413
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs17367504
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs1801131
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1801133
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.700 1.000 1 2009 2009
dbSNP: rs3818762
rs3818762
MTHFR
1 11790946 intron variant G/C snv 0.26; 1.7E-03 0.23
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs4846049
rs4846049
MTHFR ; C1orf167
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs576853093
rs576853093
MTHFR
1 11790946 intron variant -/C;CACACACACACAC ins 6.2E-03
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011