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rs35637840

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs35637840(-;-)
Make rs35637840(-;GAGTCCTTT)
Make rs35637840(GAGTCCTTT;GAGTCCTTT)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226754
GeneHBB
is asnp
is mentioned by
dbSNPrs35637840
ebirs35637840
HLIrs35637840
Exacrs35637840
Varsomers35637840
Maprs35637840
PheGenIrs35637840
hapmaprs35637840
1000 genomesrs35637840
hgdprs35637840
ensemblrs35637840
gopubmedrs35637840
geneviewrs35637840
scholarrs35637840
googlers35637840
pharmgkbrs35637840
gwascentralrs35637840
openSNPrs35637840
23andMers35637840
23andMe allrs35637840
SNP Nexus

SNPshotrs35637840
SNPdbers35637840
MSV3drs35637840
GWAS Ctlgrs35637840
Max Magnitude0
OMIM141900
Desc
Variant0198
Relatedalso
ClinVar
Risk rs35637840(GAGTCCTTTG,G;GAGTCCTTTG,G)
Alt rs35637840(GAGTCCTTTG,G;GAGTCCTTTG,G)
Reference rs35637840(AGTCCTTTG;AGTCCTTTG)
Significance Other
Disease HEMOGLOBIN NITEROI
Variation info
Gene HBB
CLNDBN HEMOGLOBIN NITEROI
Reversed 1
HGVS NC_000011.9:g.5247984_5247992delAAAGGACTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000016519.3,