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rs676785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs676785(A;A)
Make rs676785(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position25408711
GeneRHCE
is asnp
is mentioned by
dbSNPrs676785
ebirs676785
HLIrs676785
Exacrs676785
Varsomers676785
Maprs676785
PheGenIrs676785
hapmaprs676785
1000 genomesrs676785
hgdprs676785
ensemblrs676785
gopubmedrs676785
geneviewrs676785
scholarrs676785
googlers676785
pharmgkbrs676785
gwascentralrs676785
openSNPrs676785
23andMers676785
23andMe allrs676785
SNP Nexus

SNPshotrs676785
SNPdbers676785
MSV3drs676785
GWAS Ctlgrs676785
GMAF0.1221
Max Magnitude0
OMIM111700
Desc
Variant0002
Relatedalso
Rh C/c blood group


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


ClinVar
Risk rs676785(A;A)
Alt rs676785(A;A)
Reference rs676785(G;G)
Significance Non-pathogenic
Disease RH C/c POLYMORPHISM not provided
Variation info
Gene RHCE
CLNDBN RH C/c POLYMORPHISM not provided
Reversed 0
HGVS NC_000001.10:g.25735202G\x3d; NC_000001.10:g.25735202G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019283.2, RCV000144442.1,