rs35262412

Orientation

minus

Stabilized

minus

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

Make rs35262412(A;C)

Make rs35262412(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226761

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs35262412
dbSNP (classic)	rs35262412
ClinGen	rs35262412
ebi	rs35262412
HLI	rs35262412
Exac	rs35262412
Gnomad	rs35262412
Varsome	rs35262412
LitVar	rs35262412
Map	rs35262412
PheGenI	rs35262412
Biobank	rs35262412
1000 genomes	rs35262412
hgdp	rs35262412
ensembl	rs35262412
geneview	rs35262412
scholar	rs35262412
google	rs35262412
pharmgkb	rs35262412
gwascentral	rs35262412
openSNP	rs35262412
23andMe	rs35262412
SNPshot	rs35262412
SNPdbe	rs35262412
MSV3d	rs35262412
GWAS Ctlg	rs35262412

Max Magnitude

0

OMIM	141900
Desc
Variant	0083
Related	also

ClinVar
Risk	rs35262412(C;C) rs35262412(G;G)
Alt	rs35262412(C;C) rs35262412(G;G)
Reference	Rs35262412(A;A)
Significance	Other
Disease	HEMOGLOBIN G (GALVESTON) HEMOGLOBIN G (PORT ARTHUR) HEMOGLOBIN G (TEXAS)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN G (GALVESTON) HEMOGLOBIN G (PORT ARTHUR) HEMOGLOBIN G (TEXAS)
Reversed	1
HGVS	NC_000011.9:g.5247991T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016348.2, RCV000016349.2, RCV000016350.2,

[PMID 4432868] Hemoglobin S-G (S-D) syndrome.