rs1061234

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(T;T)	0	common in complete genomics

Make rs1061234(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249456

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs1061234
dbSNP (classic)	rs1061234
ClinGen	rs1061234
ebi	rs1061234
HLI	rs1061234
Exac	rs1061234
Gnomad	rs1061234
Varsome	rs1061234
LitVar	rs1061234
Map	rs1061234
PheGenI	rs1061234
Biobank	rs1061234
1000 genomes	rs1061234
hgdp	rs1061234
ensembl	rs1061234
geneview	rs1061234
scholar	rs1061234
google	rs1061234
pharmgkb	rs1061234
gwascentral	rs1061234
openSNP	rs1061234
23andMe	rs1061234
SNPshot	rs1061234
SNPdbe	rs1061234
MSV3d	rs1061234
GWAS Ctlg	rs1061234

Merged from

Rs111033586

Max Magnitude

0

OMIM	142200
Desc	HBG1 POLYMORPHISM
Variant	0001
Related	also

OMIM	142200
Desc	HEMOGLOBIN F (SARDINIA)
Variant	0018
Related	also

OMIM	142200
Desc	HEMOGLOBIN F (CHARLOTTE)
Variant	0032
Related	also

OMIM	142250
Desc	HEMOGLOBIN F (LESVOS)
Variant	0045
Related	also

OMIM	142200
Desc
Variant	0037
Related	also

OMIM	142250
Desc
Variant	0039
Related	also

ClinVar
Risk	Rs1061234(T;T)
Alt	Rs1061234(T;T)
Reference	Rs1061234(C;C)
Significance	Other
Disease	HBG1 POLYMORPHISM HEMOGLOBIN F (CHARLOTTE) HEMOGLOBIN F (PORTO TORRES) HEMOGLOBIN F (SARDINIA) not specified
Variation	info
Gene	HBG1
CLNDBN	HBG1 POLYMORPHISM HEMOGLOBIN F (CHARLOTTE) HEMOGLOBIN F (PORTO TORRES) HEMOGLOBIN F (SARDINIA) not specified
Reversed	1
HGVS	NC_000011.9:g.5270686G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016145.2, RCV000016180.1, RCV000016185.2, RCV000030904.1, RCV000455125.1,