Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs112772376
rs112772376
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs112772376
rs112772376
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11778726
rs11778726
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs16900452
rs16900452
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4466418
rs4466418
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0149745
Disease:
Oral Ulcer 		A 0.700 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455 2019
dbSNP: rs2891677
rs2891677
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0201657
Disease:
C-reactive protein measurement 		C 0.700 GeneticVariation GWASCAT Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. 30388399 2018
dbSNP: rs201447509
rs201447509
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0036341
Disease:
Schizophrenia 		ATC 0.700 GeneticVariation GWASCAT Genome-wide association study of paliperidone efficacy. 27846195 2017
dbSNP: rs757613817
rs757613817
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C4310647
Disease:
SECKEL SYNDROME 10 		A 0.700 CausalMutation CLINVAR
dbSNP: rs773917653
rs773917653
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C4310647
Disease:
SECKEL SYNDROME 10 		AAGGG 0.700 CausalMutation CLINVAR
dbSNP: rs7008482
rs7008482
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.020 GeneticVariation BEFREE SNPs rs6983561, rs7008482, and rs16901979 were significantly associated with CaP risk in WAs (P < 0.03). 22234922 2012
dbSNP: rs7008482
rs7008482
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0600139
Disease:
Prostate carcinoma 		0.020 GeneticVariation BEFREE SNPs rs6983561, rs7008482, and rs16901979 were significantly associated with CaP risk in WAs (P < 0.03). 22234922 2012
dbSNP: rs7008482
rs7008482
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.020 GeneticVariation BEFREE We report that rs7008482, which maps to the 8q24.13 region, is an additional independent prostate cancer risk variant (P = 5 x 10(-4)), and we also replicate the association of rs16901979 with prostate cancer (P = 0.002). 17978284 2007
dbSNP: rs7008482
rs7008482
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0600139
Disease:
Prostate carcinoma 		0.020 GeneticVariation BEFREE We report that rs7008482, which maps to the 8q24.13 region, is an additional independent prostate cancer risk variant (P = 5 x 10(-4)), and we also replicate the association of rs16901979 with prostate cancer (P = 0.002). 17978284 2007
dbSNP: rs7008482
rs7008482
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C1306459
Disease:
Primary malignant neoplasm 		0.010 GeneticVariation BEFREE There was little indication that 8q24 SNPs associated with other cancer types--rs7008482, rs7000448, rs6983561, rs6983267, rs13281615, rs13254738, or rs10090154--are associated with bladder cancer risk. 21051319 2010
dbSNP: rs7008482
rs7008482
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0006826
Disease:
Malignant Neoplasms 		0.010 GeneticVariation BEFREE There was little indication that 8q24 SNPs associated with other cancer types--rs7008482, rs7000448, rs6983561, rs6983267, rs13281615, rs13254738, or rs10090154--are associated with bladder cancer risk. 21051319 2010
dbSNP: rs7008482
rs7008482
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.010 GeneticVariation BEFREE We found rs7008482 in 8q24 region 4 to be significantly associated with CRC in European Americans (P = 0.03). 19520795 2009