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rs35262412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35262412(A;C)
Make rs35262412(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226761
GeneHBB
is asnp
is mentioned by
dbSNPrs35262412
ebirs35262412
HLIrs35262412
Exacrs35262412
Varsomers35262412
Maprs35262412
PheGenIrs35262412
hapmaprs35262412
1000 genomesrs35262412
hgdprs35262412
ensemblrs35262412
gopubmedrs35262412
geneviewrs35262412
scholarrs35262412
googlers35262412
pharmgkbrs35262412
gwascentralrs35262412
openSNPrs35262412
23andMers35262412
23andMe allrs35262412
SNP Nexus

SNPshotrs35262412
SNPdbers35262412
MSV3drs35262412
GWAS Ctlgrs35262412
Max Magnitude0
OMIM141900
Desc
Variant0083
Relatedalso


ClinVar
Risk rs35262412(C,G;C,G)
Alt rs35262412(C,G;C,G)
Reference rs35262412(A;A)
Significance Other
Disease HEMOGLOBIN G (GALVESTON) HEMOGLOBIN G (PORT ARTHUR) HEMOGLOBIN G (TEXAS)
Variation info
Gene HBB
CLNDBN HEMOGLOBIN G (GALVESTON) HEMOGLOBIN G (PORT ARTHUR) HEMOGLOBIN G (TEXAS)
Reversed 1
HGVS NC_000011.9:g.5247991T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016348.2, RCV000016349.2, RCV000016350.2,



[PMID 4432868] Hemoglobin S-G (S-D) syndrome.