rs41484451

Orientation

plus

Stabilized

plus

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

Make rs41484451(C;C)

Make rs41484451(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173273

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs41484451
dbSNP (classic)	rs41484451
ClinGen	rs41484451
ebi	rs41484451
HLI	rs41484451
Exac	rs41484451
Gnomad	rs41484451
Varsome	rs41484451
LitVar	rs41484451
Map	rs41484451
PheGenI	rs41484451
Biobank	rs41484451
1000 genomes	rs41484451
hgdp	rs41484451
ensembl	rs41484451
geneview	rs41484451
scholar	rs41484451
google	rs41484451
pharmgkb	rs41484451
gwascentral	rs41484451
openSNP	rs41484451
23andMe	rs41484451
SNPshot	rs41484451
SNPdbe	rs41484451
MSV3d	rs41484451
GWAS Ctlg	rs41484451

Max Magnitude

0

OMIM	141850
Desc
Variant	0066
Related	also

ClinVar
Risk	rs41484451(C;C)
Alt	rs41484451(C;C)
Reference	Rs41484451(T;T)
Significance	Other
Disease	HEMOGLOBIN PASSY
Variation	info
Gene	HBA2
CLNDBN	HEMOGLOBIN PASSY
Reversed	0
HGVS	NC_000016.9:g.223272T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016980.2,

[PMID 15768558] Two new hemoglobin variants: Hb Brem-sur-Mer [beta9(A6)Ser-->Tyr] and Hb Passy [alpha81(F2)Ser-->Pro (alpha2)].