rs35286210

Orientation

minus

Stabilized

minus

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

Make rs35286210(C;C)

Make rs35286210(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226663

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs35286210
dbSNP (classic)	rs35286210
ClinGen	rs35286210
ebi	rs35286210
HLI	rs35286210
Exac	rs35286210
Gnomad	rs35286210
Varsome	rs35286210
LitVar	rs35286210
Map	rs35286210
PheGenI	rs35286210
Biobank	rs35286210
1000 genomes	rs35286210
hgdp	rs35286210
ensembl	rs35286210
geneview	rs35286210
scholar	rs35286210
google	rs35286210
pharmgkb	rs35286210
gwascentral	rs35286210
openSNP	rs35286210
23andMe	rs35286210
SNPshot	rs35286210
SNPdbe	rs35286210
MSV3d	rs35286210
GWAS Ctlg	rs35286210

Max Magnitude

0

OMIM	141900
Desc
Variant	0396
Related	also

ClinVar
Risk	rs35286210(C;C)
Alt	rs35286210(C;C)
Reference	Rs35286210(G;G)
Significance	Other
Disease	HEMOGLOBIN CALAIS
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN CALAIS
Reversed	1
HGVS	NC_000011.9:g.5247893C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016740.2,