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rs35537181

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35537181(A;C)
Make rs35537181(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226713
GeneHBB
is asnp
is mentioned by
dbSNPrs35537181
ebirs35537181
HLIrs35537181
Exacrs35537181
Varsomers35537181
Maprs35537181
PheGenIrs35537181
hapmaprs35537181
1000 genomesrs35537181
hgdprs35537181
ensemblrs35537181
gopubmedrs35537181
geneviewrs35537181
scholarrs35537181
googlers35537181
pharmgkbrs35537181
gwascentralrs35537181
openSNPrs35537181
23andMers35537181
23andMe allrs35537181
SNP Nexus

SNPshotrs35537181
SNPdbers35537181
MSV3drs35537181
GWAS Ctlgrs35537181
Max Magnitude0
OMIM141900
Desc
Variant0132
Relatedalso


ClinVar
Risk rs35537181(C;C)
Alt rs35537181(C;C)
Reference rs35537181(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene HBB
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.5247943T>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016418.3,



[PMID 5032420] Fast haemoglobin variant found in Hawaiian-Chinese-Caucasian family in Hawaii and a Chinese subject in taiwan.


[PMID 5553980] Hemoglobin J Kaohsiung: beta 59 Lys--Thr.