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rs609320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs609320(C;G)
Make rs609320(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position25390874
GeneRHCE
is asnp
is mentioned by
dbSNPrs609320
ebirs609320
HLIrs609320
Exacrs609320
Varsomers609320
Maprs609320
PheGenIrs609320
hapmaprs609320
1000 genomesrs609320
hgdprs609320
ensemblrs609320
gopubmedrs609320
geneviewrs609320
scholarrs609320
googlers609320
pharmgkbrs609320
gwascentralrs609320
openSNPrs609320
23andMers609320
23andMe allrs609320
SNP Nexus

SNPshotrs609320
SNPdbers609320
MSV3drs609320
GWAS Ctlgrs609320
Merged fromRs121912764
GMAF0.1621
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM111700
Desc
Variant0001
Relatedalso


ClinVar
Risk rs609320(G;G)
Alt rs609320(G;G)
Reference Rs609320(C;C)
Significance Non-pathogenic
Disease RH E/e POLYMORPHISM
Variation info
Gene RHCE
CLNDBN RH E/e POLYMORPHISM
Reversed 0
HGVS NC_000001.10:g.25717365C\x3d
CLNSRC OMIM Allelic Variant
CLNACC RCV000019282.2,



[PMID 21257350OA-icon.png] DNA-based methods in the immunohematology reference laboratory.


GET Evidence
RHCE-A226P
aa_change Ala226Pro
aa_change_short A226P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.141011
summary


Rh E/e blood group