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rs35492035

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35492035(C;C)
Make rs35492035(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225636
GeneHBB
is asnp
is mentioned by
dbSNPrs35492035
ebirs35492035
HLIrs35492035
Exacrs35492035
Varsomers35492035
Maprs35492035
PheGenIrs35492035
hapmaprs35492035
1000 genomesrs35492035
hgdprs35492035
ensemblrs35492035
gopubmedrs35492035
geneviewrs35492035
scholarrs35492035
googlers35492035
pharmgkbrs35492035
gwascentralrs35492035
openSNPrs35492035
23andMers35492035
23andMe allrs35492035
SNP Nexus

SNPshotrs35492035
SNPdbers35492035
MSV3drs35492035
GWAS Ctlgrs35492035
Max Magnitude0
OMIM141900
Desc
Variant0007
Relatedalso


ClinVar
Risk rs35492035(C;C)
Alt rs35492035(C;C)
Reference rs35492035(G;G)
Significance Other
Disease HEMOGLOBIN ALTDORF
Variation info
Gene HBB
CLNDBN HEMOGLOBIN ALTDORF
Reversed 1
HGVS NC_000011.9:g.5246866C>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016248.2,



[PMID 1261680] Hb Altdorf alpha2beta2 135 (H13) Ala leads to Pro: a new electrophoretically silent unstable haemoglobin variant from Switzerland.