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rs11276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11276(A;A)
Make rs11276(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position14840505
GeneART4
is asnp
is mentioned by
dbSNPrs11276
ebirs11276
HLIrs11276
Exacrs11276
Varsomers11276
Maprs11276
PheGenIrs11276
hapmaprs11276
1000 genomesrs11276
hgdprs11276
ensemblrs11276
gopubmedrs11276
geneviewrs11276
scholarrs11276
googlers11276
pharmgkbrs11276
gwascentralrs11276
openSNPrs11276
23andMers11276
23andMe allrs11276
SNP Nexus

SNPshotrs11276
SNPdbers11276
MSV3drs11276
GWAS Ctlgrs11276
GMAF0.2801
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM110600
DescDOMBROCK BLOOD GROUP
Variant0001
Relatedalso


ClinVar
Risk rs11276(A;A)
Alt rs11276(A;A)
Reference rs11276(G;G)
Significance Other
Disease Blood group
Variation info
Gene ART4
CLNDBN Blood group, Dombrock system
Reversed 1
HGVS NC_000012.11:g.14993439C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019304.29,



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


GET Evidence
ART4-D265N
aa_change Asp265Asn
aa_change_short D265N
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.353411
summary



{{on chip | Illumina Human 1M}

This SNP is associated with the Dombrock blood group [PMID 11001920]