rs41404150

Orientation

minus

Stabilized

minus

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

Make rs41404150(C;G)

Make rs41404150(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249573

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs41404150
dbSNP (classic)	rs41404150
ClinGen	rs41404150
ebi	rs41404150
HLI	rs41404150
Exac	rs41404150
Gnomad	rs41404150
Varsome	rs41404150
LitVar	rs41404150
Map	rs41404150
PheGenI	rs41404150
Biobank	rs41404150
1000 genomes	rs41404150
hgdp	rs41404150
ensembl	rs41404150
geneview	rs41404150
scholar	rs41404150
google	rs41404150
pharmgkb	rs41404150
gwascentral	rs41404150
openSNP	rs41404150
23andMe	rs41404150
SNPshot	rs41404150
SNPdbe	rs41404150
MSV3d	rs41404150
GWAS Ctlg	rs41404150

Max Magnitude

0

OMIM	142200
Desc
Variant	0016
Related	also

ClinVar
Risk	rs41404150(G;G)
Alt	rs41404150(G;G)
Reference	Rs41404150(C;C)
Significance	Other
Disease	HEMOGLOBIN F (PENDERGRASS)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (PENDERGRASS)
Reversed	1
HGVS	NC_000011.9:g.5270803G>C
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016160.1,

[PMID 2581920] Hb F-Pendergrass, an A gamma I variant with a Pro----Arg substitution at position gamma 36(C2).