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rs35198910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35198910(C;C)
Make rs35198910(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226995
GeneHBB
is asnp
is mentioned by
dbSNPrs35198910
ebirs35198910
HLIrs35198910
Exacrs35198910
Varsomers35198910
Maprs35198910
PheGenIrs35198910
hapmaprs35198910
1000 genomesrs35198910
hgdprs35198910
ensemblrs35198910
gopubmedrs35198910
geneviewrs35198910
scholarrs35198910
googlers35198910
pharmgkbrs35198910
gwascentralrs35198910
openSNPrs35198910
23andMers35198910
23andMe allrs35198910
SNP Nexus

SNPshotrs35198910
SNPdbers35198910
MSV3drs35198910
GWAS Ctlgrs35198910
Max Magnitude0
OMIM141900
Desc
Variant0504
Relatedalso


ClinVar
Risk rs35198910(C;C)
Alt rs35198910(C;C)
Reference rs35198910(G;G)
Significance Other
Disease HEMOGLOBIN LIMASSOL
Variation info
Gene HBB
CLNDBN HEMOGLOBIN LIMASSOL
Reversed 1
HGVS NC_000011.9:g.5248225C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016860.2,



[PMID 11791876] Hb Limassol [beta8(A5)Lys-->Asn]: a new hemoglobin variant.