Have questions? Visit https://www.reddit.com/r/SNPedia

rs35658323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35658323(C;C)
Make rs35658323(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225663
GeneHBB
is asnp
is mentioned by
dbSNPrs35658323
ebirs35658323
HLIrs35658323
Exacrs35658323
Varsomers35658323
Maprs35658323
PheGenIrs35658323
hapmaprs35658323
1000 genomesrs35658323
hgdprs35658323
ensemblrs35658323
gopubmedrs35658323
geneviewrs35658323
scholarrs35658323
googlers35658323
pharmgkbrs35658323
gwascentralrs35658323
openSNPrs35658323
23andMers35658323
23andMe allrs35658323
SNP Nexus

SNPshotrs35658323
SNPdbers35658323
MSV3drs35658323
GWAS Ctlgrs35658323
Max Magnitude0
OMIM141900
Desc
Variant0508
Relatedalso


ClinVar
Risk rs35658323(C;C)
Alt rs35658323(C;C)
Reference rs35658323(G;G)
Significance Other
Disease HEMOGLOBIN MOLFETTA
Variation info
Gene HBB
CLNDBN HEMOGLOBIN MOLFETTA
Reversed 1
HGVS NC_000011.9:g.5246893C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016864.2,



[PMID 11939515] Hb Molfetta [beta126(H4)Val-->Leu, GTG-->CTG]: a new, silent, neutral beta chain variant found in an Italian woman.