rs34866629

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs34866629(A;G)

Make rs34866629(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226964

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs34866629
dbSNP (classic)	rs34866629
ClinGen	rs34866629
ebi	rs34866629
HLI	rs34866629
Exac	rs34866629
Gnomad	rs34866629
Varsome	rs34866629
LitVar	rs34866629
Map	rs34866629
PheGenI	rs34866629
Biobank	rs34866629
1000 genomes	rs34866629
hgdp	rs34866629
ensembl	rs34866629
geneview	rs34866629
scholar	rs34866629
google	rs34866629
pharmgkb	rs34866629
gwascentral	rs34866629
openSNP	rs34866629
23andMe	rs34866629
SNPshot	rs34866629
SNPdbe	rs34866629
MSV3d	rs34866629
GWAS Ctlg	rs34866629

Max Magnitude

0

OMIM	141900
Desc
Variant	0005
Related	also

ClinVar
Risk	rs34866629(G;G)
Alt	rs34866629(G;G)
Reference	Rs34866629(A;A)
Significance	Other
Disease	HEMOGLOBIN ALAMO
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN ALAMO
Reversed	1
HGVS	NC_000011.9:g.5248194T>C
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016246.3,

[PMID 914645] Hemoglobin Alamo (alpha2beta2 19 (b1) Asn replaced by Asp).