FCHSD2, FCH and double SH3 domains 2, 9873

N. diseases: 5; N. variants: 4
Source: CURATED ×
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: rs72981516
rs72981516 		1.000 0.040 11 72959855 intron variant T/G snv 6.2E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs11235654
rs11235654 		11 73094817 intron variant A/G snv 0.17
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs117610694
rs117610694 		1.000 0.080 11 73070209 intron variant C/T snv 9.6E-03
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2018 2018
dbSNP: rs1783598
rs1783598 		1.000 0.080 11 73140418 intron variant C/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1783598
rs1783598 		1.000 0.080 11 73140418 intron variant C/G;T snv
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result 		0.700 1.000 1 2012 2012
dbSNP: rs1783598
rs1783598 		1.000 0.080 11 73140418 intron variant C/G;T snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.700 1.000 1 2012 2012