rs41330850

Orientation

minus

Stabilized

minus

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

Make rs41330850(A;A)

Make rs41330850(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5248418

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs41330850
dbSNP (classic)	rs41330850
ClinGen	rs41330850
ebi	rs41330850
HLI	rs41330850
Exac	rs41330850
Gnomad	rs41330850
Varsome	rs41330850
LitVar	rs41330850
Map	rs41330850
PheGenI	rs41330850
Biobank	rs41330850
1000 genomes	rs41330850
hgdp	rs41330850
ensembl	rs41330850
geneview	rs41330850
scholar	rs41330850
google	rs41330850
pharmgkb	rs41330850
gwascentral	rs41330850
openSNP	rs41330850
23andMe	rs41330850
SNPshot	rs41330850
SNPdbe	rs41330850
MSV3d	rs41330850
GWAS Ctlg	rs41330850

Max Magnitude

0

OMIM	142200
Desc
Variant	0002
Related	also

ClinVar
Risk	rs41330850(A;A)
Alt	rs41330850(A;A)
Reference	Rs41330850(G;G)
Significance	Other
Disease	HEMOGLOBIN F (BASKENT)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (BASKENT)
Reversed	1
HGVS	NC_000011.9:g.5269648C>T
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016146.1,

[PMID 2454900] Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.