MEIS1, Meis homeobox 1, 4211

N. diseases: 104; N. variants: 19
Disease: Electrocardiogram ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3891585
rs3891585 		2 66529844 intron variant A/C;G snv
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.800 1.000 3 2011 2019
dbSNP: rs10865355
rs10865355 		2 66537865 intron variant A/G snv 0.61
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.800 1.000 2 2011 2019
dbSNP: rs11897119
rs11897119 		2 66544868 intron variant T/A;C snv
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.800 1.000 2 2010 2019
dbSNP: rs11677371
rs11677371 		2 66529281 intron variant A/G;T snv
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2011 2011
dbSNP: rs4430933
rs4430933 		2 66522478 intron variant A/G snv 0.58
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2018 2018
dbSNP: rs4433986
rs4433986 		2 66533179 intron variant A/G snv 0.59
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2011 2011
dbSNP: rs6724747
rs6724747 		2 66522696 intron variant G/A snv 0.23
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2019 2019
dbSNP: rs7603236
rs7603236 		2 66535279 intron variant C/T snv 0.61
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2011 2011