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: rs2946834
rs2946834
HELLPAR ; LINC02456
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63
CUI: C0027092
Disease: Myopia
Myopia 		0.010 1.000 1 2011 2011
dbSNP: rs2946834
rs2946834
HELLPAR ; LINC02456
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63
CUI: C1960398
Disease: HER2-positive carcinoma of breast
HER2-positive carcinoma of breast 		0.010 1.000 1 2013 2013
dbSNP: rs2946834
rs2946834
HELLPAR ; LINC02456
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63
CUI: C0280280
Disease: stage, prostate cancer
stage, prostate cancer 		0.010 1.000 1 2013 2013
dbSNP: rs2946834
rs2946834
HELLPAR ; LINC02456
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 < 0.001 1 2011 2011
dbSNP: rs2946834
rs2946834
HELLPAR ; LINC02456
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs2946834
rs2946834
HELLPAR ; LINC02456
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2013 2013
dbSNP: rs2946834
rs2946834
HELLPAR ; LINC02456
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2013 2013