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rs786205441

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205441(G;T)
Make rs786205441(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position16133226
GeneEPHA2
is asnp
is mentioned by
dbSNPrs786205441
ebirs786205441
HLIrs786205441
Exacrs786205441
Varsomers786205441
Maprs786205441
PheGenIrs786205441
hapmaprs786205441
1000 genomesrs786205441
hgdprs786205441
ensemblrs786205441
gopubmedrs786205441
geneviewrs786205441
scholarrs786205441
googlers786205441
pharmgkbrs786205441
gwascentralrs786205441
openSNPrs786205441
23andMers786205441
23andMe allrs786205441
SNP Nexus

SNPshotrs786205441
SNPdbers786205441
MSV3drs786205441
GWAS Ctlgrs786205441
Max Magnitude0
ClinVar
Risk rs786205441(T;T)
Alt rs786205441(T;T)
Reference rs786205441(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EPHA2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.16459721C>A
CLNSRC
CLNACC RCV000171149.1,