rs34149886

Orientation

minus

Stabilized

minus

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

Make rs34149886(A;G)

Make rs34149886(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5232968

Gene

HBD

is a	snp
is	mentioned by
dbSNP	rs34149886
dbSNP (classic)	rs34149886
ClinGen	rs34149886
ebi	rs34149886
HLI	rs34149886
Exac	rs34149886
Gnomad	rs34149886
Varsome	rs34149886
LitVar	rs34149886
Map	rs34149886
PheGenI	rs34149886
Biobank	rs34149886
1000 genomes	rs34149886
hgdp	rs34149886
ensembl	rs34149886
geneview	rs34149886
scholar	rs34149886
google	rs34149886
pharmgkb	rs34149886
gwascentral	rs34149886
openSNP	rs34149886
23andMe	rs34149886
SNPshot	rs34149886
SNPdbe	rs34149886
MSV3d	rs34149886
GWAS Ctlg	rs34149886

Max Magnitude

0

OMIM	142000
Desc
Variant	0038
Related	also

ClinVar
Risk	rs34149886(G;G) rs34149886(T;T)
Alt	rs34149886(G;G) rs34149886(T;T)
Reference	Rs34149886(A;A)
Significance	Other
Disease	HEMOGLOBIN A(2) MONREALE
Variation	info
Gene	HBD
CLNDBN	HEMOGLOBIN A(2) MONREALE
Reversed	1
HGVS	NC_000011.9:g.5254198T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016232.1,

[PMID 11939506] Hb A2-Monreale [delta146(HC3)His-->Arg], a novel delta chain variant detected in west Sicily.