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rs35666685

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35666685(A;A)
Make rs35666685(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5234132
GeneHBD
is asnp
is mentioned by
dbSNPrs35666685
dbSNP (classic)rs35666685
ClinGenrs35666685
ebirs35666685
HLIrs35666685
Exacrs35666685
Gnomadrs35666685
Varsomers35666685
LitVarrs35666685
Maprs35666685
PheGenIrs35666685
Biobankrs35666685
1000 genomesrs35666685
hgdprs35666685
ensemblrs35666685
geneviewrs35666685
scholarrs35666685
googlers35666685
pharmgkbrs35666685
gwascentralrs35666685
openSNPrs35666685
23andMers35666685
SNPshotrs35666685
SNPdbers35666685
MSV3drs35666685
GWAS Ctlgrs35666685
Max Magnitude0
OMIM142000
Desc
Variant0040
Relatedalso


ClinVar
Risk rs35666685(A;A) rs35666685(T;T)
Alt rs35666685(A;A) rs35666685(T;T)
Reference Rs35666685(C;C)
Significance Other
Disease HEMOGLOBIN A(2) CAMPANIA
Variation info
Gene HBD
CLNDBN HEMOGLOBIN A(2) CAMPANIA
Reversed 1
HGVS NC_000011.9:g.5255362G>T
CLNSRC HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000016234.1,



[PMID 12402333] Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features.