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: rs9909004
rs9909004
PRKCA
0.925 0.040 17 66310015 intron variant C/T snv 0.59
CUI: C0018801
Disease: Heart failure
Heart failure 		0.020 1.000 2 2017 2019
dbSNP: rs9909004
rs9909004
PRKCA
0.925 0.040 17 66310015 intron variant C/T snv 0.59
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.020 1.000 2 2017 2019
dbSNP: rs11079657
rs11079657
PRKCA
1.000 0.080 17 66435948 intron variant A/G snv 0.63
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2009 2009
dbSNP: rs121917733
rs121917733
PRKCA
1.000 0.040 17 66689010 missense variant A/G snv
CUI: C0007133
Disease: Carcinoma, Papillary
Carcinoma, Papillary 		0.010 1.000 1 2002 2002
dbSNP: rs16960228
rs16960228
PRKCA
1.000 0.040 17 66792709 intron variant G/A snv 0.13
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.010 1.000 1 2013 2013
dbSNP: rs7342847
rs7342847
PRKCA
0.925 0.080 17 66806426 3 prime UTR variant C/T snv 0.39
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2009 2009
dbSNP: rs7342847
rs7342847
PRKCA
0.925 0.080 17 66806426 3 prime UTR variant C/T snv 0.39
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs8074995
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		0.010 1.000 1 2011 2011
dbSNP: rs8074995
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13
CUI: C0542476
Disease: Forgetful
Forgetful 		0.010 1.000 1 2011 2011
dbSNP: rs8074995
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13
CUI: C0233794
Disease: Memory impairment
Memory impairment 		0.010 1.000 1 2011 2011
dbSNP: rs8074995
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2011 2011
dbSNP: rs8074995
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2011 2011
dbSNP: rs9303504
rs9303504
PRKCA
0.925 0.040 17 66319248 intron variant G/C snv 0.59
CUI: C0018801
Disease: Heart failure
Heart failure 		0.010 1.000 1 2019 2019
dbSNP: rs9303504
rs9303504
PRKCA
0.925 0.040 17 66319248 intron variant G/C snv 0.59
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.010 1.000 1 2019 2019
dbSNP: rs9892651
rs9892651
PRKCA
17 66307675 intron variant C/T snv 0.59
CUI: C0043144
Disease: Wheezing
Wheezing 		0.010 1.000 1 2016 2016