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rs587776864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776864(C;T)
Make rs587776864(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position5254405
GeneHBG2
is asnp
is mentioned by
dbSNPrs587776864
ebirs587776864
HLIrs587776864
Exacrs587776864
Varsomers587776864
Maprs587776864
PheGenIrs587776864
hapmaprs587776864
1000 genomesrs587776864
hgdprs587776864
ensemblrs587776864
gopubmedrs587776864
geneviewrs587776864
scholarrs587776864
googlers587776864
pharmgkbrs587776864
gwascentralrs587776864
openSNPrs587776864
23andMers587776864
23andMe allrs587776864
SNP Nexus

SNPshotrs587776864
SNPdbers587776864
MSV3drs587776864
GWAS Ctlgrs587776864
Max Magnitude0
ClinVar
Risk rs587776864(C,T;C,T)
Alt rs587776864(C,T;C,T)
Reference rs587776864(G;G)
Significance Pathogenic
Disease Cyanosis
Variation info
Gene HBG2
CLNDBN Cyanosis, transient neonatal
Reversed 1
HGVS NC_000011.9:g.5275635C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022615.23,