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rs35700518

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35700518(G;G)
Make rs35700518(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249571
GeneHBG1
is asnp
is mentioned by
dbSNPrs35700518
ebirs35700518
HLIrs35700518
Exacrs35700518
Varsomers35700518
Maprs35700518
PheGenIrs35700518
hapmaprs35700518
1000 genomesrs35700518
hgdprs35700518
ensemblrs35700518
gopubmedrs35700518
geneviewrs35700518
scholarrs35700518
googlers35700518
pharmgkbrs35700518
gwascentralrs35700518
openSNPrs35700518
23andMers35700518
23andMe allrs35700518
SNP Nexus

SNPshotrs35700518
SNPdbers35700518
MSV3drs35700518
GWAS Ctlgrs35700518
Max Magnitude0
OMIM142200
Desc
Variant0006
Relatedalso
ClinVar
Risk rs35700518(G;G)
Alt rs35700518(G;G)
Reference rs35700518(T;T)
Significance Other
Disease HEMOGLOBIN F (COBB)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (COBB)
Reversed 1
HGVS NC_000011.9:g.5270801A>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016150.1,



[PMID 2419280] Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly.