rs34127117

Orientation

minus

Stabilized

minus

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

Make rs34127117(A;G)

Make rs34127117(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249390

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs34127117
dbSNP (classic)	rs34127117
ClinGen	rs34127117
ebi	rs34127117
HLI	rs34127117
Exac	rs34127117
Gnomad	rs34127117
Varsome	rs34127117
LitVar	rs34127117
Map	rs34127117
PheGenI	rs34127117
Biobank	rs34127117
1000 genomes	rs34127117
hgdp	rs34127117
ensembl	rs34127117
geneview	rs34127117
scholar	rs34127117
google	rs34127117
pharmgkb	rs34127117
gwascentral	rs34127117
openSNP	rs34127117
23andMe	rs34127117
SNPshot	rs34127117
SNPdbe	rs34127117
MSV3d	rs34127117
GWAS Ctlg	rs34127117

Max Magnitude

0

OMIM	142200
Desc
Variant	0008
Related	also

ClinVar
Risk	rs34127117(G;G)
Alt	rs34127117(G;G)
Reference	Rs34127117(A;A)
Significance	Other
Disease	HEMOGLOBIN F (DICKINSON)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (DICKINSON)
Reversed	1
HGVS	NC_000011.9:g.5270620T>C
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016152.1,