Source: BEFREE

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: rs41291957
rs41291957
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 1.000 1 2019 2019
dbSNP: rs41291957
rs41291957
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.010 1.000 1 2014 2014
dbSNP: rs41291957
rs41291957
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs41291957
rs41291957
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs41291957
rs41291957
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2014 2014
dbSNP: rs41291957
rs41291957
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs41291957
rs41291957
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2013 2013