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rs35848600

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35848600(A;A)
Make rs35848600(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5232980
GeneHBD
is asnp
is mentioned by
dbSNPrs35848600
ebirs35848600
HLIrs35848600
Exacrs35848600
Varsomers35848600
Maprs35848600
PheGenIrs35848600
hapmaprs35848600
1000 genomesrs35848600
hgdprs35848600
ensemblrs35848600
gopubmedrs35848600
geneviewrs35848600
scholarrs35848600
googlers35848600
pharmgkbrs35848600
gwascentralrs35848600
openSNPrs35848600
23andMers35848600
23andMe allrs35848600
SNP Nexus

SNPshotrs35848600
SNPdbers35848600
MSV3drs35848600
GWAS Ctlgrs35848600
Max Magnitude0
? (A;A) (A;C) (C;C) 28
OMIM142000
Desc
Variant0006
Relatedalso


ClinVar
Risk rs35848600(A;A)
Alt rs35848600(A;A)
Reference rs35848600(C;C)
Significance Other
Disease HEMOGLOBIN A(2) FITZROY
Variation info
Gene HBD
CLNDBN HEMOGLOBIN A(2) FITZROY
Reversed 1
HGVS NC_000011.9:g.5254210G>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016192.1,



[PMID 6548205] Hemoglobin A2 Fitzroy delta 142 Ala----Asp: a new delta-chain variant.