rs35848600

Orientation

minus

Stabilized

minus

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

Make rs35848600(A;A)

Make rs35848600(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5232980

Gene

HBD

is a	snp
is	mentioned by
dbSNP	rs35848600
dbSNP (classic)	rs35848600
ClinGen	rs35848600
ebi	rs35848600
HLI	rs35848600
Exac	rs35848600
Gnomad	rs35848600
Varsome	rs35848600
LitVar	rs35848600
Map	rs35848600
PheGenI	rs35848600
Biobank	rs35848600
1000 genomes	rs35848600
hgdp	rs35848600
ensembl	rs35848600
geneview	rs35848600
scholar	rs35848600
google	rs35848600
pharmgkb	rs35848600
gwascentral	rs35848600
openSNP	rs35848600
23andMe	rs35848600
SNPshot	rs35848600
SNPdbe	rs35848600
MSV3d	rs35848600
GWAS Ctlg	rs35848600

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

OMIM	142000
Desc
Variant	0006
Related	also

ClinVar
Risk	rs35848600(A;A)
Alt	rs35848600(A;A)
Reference	Rs35848600(C;C)
Significance	Other
Disease	HEMOGLOBIN A(2) FITZROY
Variation	info
Gene	HBD
CLNDBN	HEMOGLOBIN A(2) FITZROY
Reversed	1
HGVS	NC_000011.9:g.5254210G>T
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016192.1,

[PMID 6548205] Hemoglobin A2 Fitzroy delta 142 Ala----Asp: a new delta-chain variant.