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rs8176038

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs8176038(C;C)
Make rs8176038(C;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position142943026
GeneKEL
is asnp
is mentioned by
dbSNPrs8176038
ebirs8176038
HLIrs8176038
Exacrs8176038
Varsomers8176038
Maprs8176038
PheGenIrs8176038
hapmaprs8176038
1000 genomesrs8176038
hgdprs8176038
ensemblrs8176038
gopubmedrs8176038
geneviewrs8176038
scholarrs8176038
googlers8176038
pharmgkbrs8176038
gwascentralrs8176038
openSNPrs8176038
23andMers8176038
23andMe allrs8176038
SNP Nexus

SNPshotrs8176038
SNPdbers8176038
MSV3drs8176038
GWAS Ctlgrs8176038
GMAF0.02296
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs8176038(C;C)
Alt rs8176038(C;C)
Reference rs8176038(T;T)
Significance Pathogenic
Disease Kel6 antigen
Variation info
Gene KEL
CLNDBN Kel6 antigen
Reversed 1
HGVS NC_000007.13:g.142640113A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024078.2,



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