rs587776864

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0	common in clinvar

Make rs587776864(C;T)

Make rs587776864(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

5254405

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs587776864
dbSNP (classic)	rs587776864
ClinGen	rs587776864
ebi	rs587776864
HLI	rs587776864
Exac	rs587776864
Gnomad	rs587776864
Varsome	rs587776864
LitVar	rs587776864
Map	rs587776864
PheGenI	rs587776864
Biobank	rs587776864
1000 genomes	rs587776864
hgdp	rs587776864
ensembl	rs587776864
geneview	rs587776864
scholar	rs587776864
google	rs587776864
pharmgkb	rs587776864
gwascentral	rs587776864
openSNP	rs587776864
23andMe	rs587776864
SNPshot	rs587776864
SNPdbe	rs587776864
MSV3d	rs587776864
GWAS Ctlg	rs587776864

Max Magnitude

0

ClinVar
Risk	Rs587776864(C;C) rs587776864(T;T)
Alt	Rs587776864(C;C) rs587776864(T;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 UniProtKB (protein)
CLNACC	RCV000022615.23,