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rs2278107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2278107(C;C)
Make rs2278107(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position93410921
GeneEPHA7
is asnp
is mentioned by
dbSNPrs2278107
ebirs2278107
HLIrs2278107
Exacrs2278107
Varsomers2278107
Maprs2278107
PheGenIrs2278107
hapmaprs2278107
1000 genomesrs2278107
hgdprs2278107
ensemblrs2278107
gopubmedrs2278107
geneviewrs2278107
scholarrs2278107
googlers2278107
pharmgkbrs2278107
gwascentralrs2278107
openSNPrs2278107
23andMers2278107
23andMe allrs2278107
SNP Nexus

SNPshotrs2278107
SNPdbers2278107
MSV3drs2278107
GWAS Ctlgrs2278107
GMAF0.06474
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 20085586] Genome-wide identification of chemosensitive single nucleotide polymorphism markers in colorectal cancers


[PMID 18853455OA-icon.png] Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.


GET Evidence
EPHA7-I138V
aa_change Ile138Val
aa_change_short I138V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0218442
summary