rs35198910

Orientation

minus

Stabilized

minus

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

Make rs35198910(C;C)

Make rs35198910(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226995

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs35198910
dbSNP (classic)	rs35198910
ClinGen	rs35198910
ebi	rs35198910
HLI	rs35198910
Exac	rs35198910
Gnomad	rs35198910
Varsome	rs35198910
LitVar	rs35198910
Map	rs35198910
PheGenI	rs35198910
Biobank	rs35198910
1000 genomes	rs35198910
hgdp	rs35198910
ensembl	rs35198910
geneview	rs35198910
scholar	rs35198910
google	rs35198910
pharmgkb	rs35198910
gwascentral	rs35198910
openSNP	rs35198910
23andMe	rs35198910
SNPshot	rs35198910
SNPdbe	rs35198910
MSV3d	rs35198910
GWAS Ctlg	rs35198910

Max Magnitude

0

OMIM	141900
Desc
Variant	0504
Related	also

ClinVar
Risk	rs35198910(C;C)
Alt	rs35198910(C;C)
Reference	Rs35198910(G;G)
Significance	Other
Disease	HEMOGLOBIN LIMASSOL
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN LIMASSOL
Reversed	1
HGVS	NC_000011.9:g.5248225C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016860.2,

[PMID 11791876] Hb Limassol [beta8(A5)Lys-->Asn]: a new hemoglobin variant.