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rs750565190

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs750565190(C;C)
Make rs750565190(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position5741783
GeneEVC
is asnp
is mentioned by
dbSNPrs750565190
ebirs750565190
HLIrs750565190
Exacrs750565190
Varsomers750565190
Maprs750565190
PheGenIrs750565190
hapmaprs750565190
1000 genomesrs750565190
hgdprs750565190
ensemblrs750565190
gopubmedrs750565190
geneviewrs750565190
scholarrs750565190
googlers750565190
pharmgkbrs750565190
gwascentralrs750565190
openSNPrs750565190
23andMers750565190
23andMe allrs750565190
SNP Nexus

SNPshotrs750565190
SNPdbers750565190
MSV3drs750565190
GWAS Ctlgrs750565190
Max Magnitude0
ClinVar
Risk rs750565190(C;C)
Alt rs750565190(C;C)
Reference rs750565190(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EVC
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.5743510T>A
CLNSRC
CLNACC RCV000171373.1,