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rs34188626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34188626(C;C)
Make rs34188626(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225646
GeneHBB
is asnp
is mentioned by
dbSNPrs34188626
ebirs34188626
HLIrs34188626
Exacrs34188626
Varsomers34188626
Maprs34188626
PheGenIrs34188626
hapmaprs34188626
1000 genomesrs34188626
hgdprs34188626
ensemblrs34188626
gopubmedrs34188626
geneviewrs34188626
scholarrs34188626
googlers34188626
pharmgkbrs34188626
gwascentralrs34188626
openSNPrs34188626
23andMers34188626
23andMe allrs34188626
SNP Nexus

SNPshotrs34188626
SNPdbers34188626
MSV3drs34188626
GWAS Ctlgrs34188626
Max Magnitude0
OMIM141900
Desc
Variant0476
Relatedalso


ClinVar
Risk rs34188626(C;C)
Alt rs34188626(C;C)
Reference rs34188626(G;G)
Significance Other
Disease HEMOGLOBIN SILVER SPRINGS
Variation info
Gene HBB
CLNDBN HEMOGLOBIN SILVER SPRINGS
Reversed 1
HGVS NC_000011.9:g.5246876C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016830.2,



[PMID 9494046] Hb Silver Springs [beta 131(H9)Gln-->His], a new hemoglobin variant found in six African-Americans.