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rs6678616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs6678616(C;T)
Make rs6678616(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position16148628
GeneEPHA2
is asnp
is mentioned by
dbSNPrs6678616
dbSNP (classic)rs6678616
ClinGenrs6678616
ebirs6678616
HLIrs6678616
Exacrs6678616
Gnomadrs6678616
Varsomers6678616
LitVarrs6678616
Maprs6678616
PheGenIrs6678616
Biobankrs6678616
1000 genomesrs6678616
hgdprs6678616
ensemblrs6678616
geneviewrs6678616
scholarrs6678616
googlers6678616
pharmgkbrs6678616
gwascentralrs6678616
openSNPrs6678616
23andMers6678616
SNPshotrs6678616
SNPdbers6678616
MSV3drs6678616
GWAS Ctlgrs6678616
GMAF0.2296
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM176946
DescEPHRIN RECEPTOR EphA2; EPHA2
Variant
Relatedalso

[PMID 19649315OA-icon.png] EPHA2 is associated with age-related cortical cataract in mice and humans

OMIM613020
Desc
Variant
Relatedalso


ClinVar
Risk rs6678616(T;T)
Alt rs6678616(T;T)
Reference Rs6678616(C;C)
Significance Non-pathogenic
Disease not specified Age-related cortical cataract
Variation info
Gene EPHA2
CLNDBN not specified Age-related cortical cataract
Reversed 0
HGVS NC_000001.10:g.16475123C>T
CLNSRC
CLNACC RCV000253199.1, RCV000309096.1,