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rs35461710

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Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35461710(C;T)
Make rs35461710(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225669
GeneHBB
is asnp
is mentioned by
dbSNPrs35461710
ebirs35461710
HLIrs35461710
Exacrs35461710
Varsomers35461710
Maprs35461710
PheGenIrs35461710
hapmaprs35461710
1000 genomesrs35461710
hgdprs35461710
ensemblrs35461710
gopubmedrs35461710
geneviewrs35461710
scholarrs35461710
googlers35461710
pharmgkbrs35461710
gwascentralrs35461710
openSNPrs35461710
23andMers35461710
23andMe allrs35461710
SNP Nexus

SNPshotrs35461710
SNPdbers35461710
MSV3drs35461710
GWAS Ctlgrs35461710
Max Magnitude0
OMIM141900
Desc
Variant0288
Relatedalso


ClinVar
Risk rs35461710(T;T)
Alt rs35461710(T;T)
Reference rs35461710(C;C)
Significance Other
Disease HEMOGLOBIN TUNIS
Variation info
Gene HBB
CLNDBN HEMOGLOBIN TUNIS
Reversed 1
HGVS NC_000011.9:g.5246899G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016631.2,



[PMID 3384695] Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLC.