PLCE1, phospholipase C epsilon 1, 51196

N. diseases: 114; N. variants: 57
Disease: Stomach Carcinoma ×
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: rs3781264
rs3781264 		0.851 0.120 10 94310618 intron variant A/G snv 0.25
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.710 1.000 2 2010 2012
dbSNP: rs10509671
rs10509671 		1.000 0.080 10 94309297 intron variant T/G snv 0.24
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2020 2020
dbSNP: rs2274223
rs2274223 		0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.100 1.000 16 2010 2019
dbSNP: rs11187842
rs11187842 		0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2012 2014
dbSNP: rs3765524
rs3765524 		0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2012 2019
dbSNP: rs753724
rs753724 		0.882 0.080 10 94291660 intron variant G/A;C;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2012 2014
dbSNP: rs10509670
rs10509670 		0.851 0.080 10 94308190 intron variant A/G snv 0.30
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019