rs35700518

Orientation

minus

Stabilized

minus

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

Make rs35700518(G;G)

Make rs35700518(G;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249571

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs35700518
dbSNP (classic)	rs35700518
ClinGen	rs35700518
ebi	rs35700518
HLI	rs35700518
Exac	rs35700518
Gnomad	rs35700518
Varsome	rs35700518
LitVar	rs35700518
Map	rs35700518
PheGenI	rs35700518
Biobank	rs35700518
1000 genomes	rs35700518
hgdp	rs35700518
ensembl	rs35700518
geneview	rs35700518
scholar	rs35700518
google	rs35700518
pharmgkb	rs35700518
gwascentral	rs35700518
openSNP	rs35700518
23andMe	rs35700518
SNPshot	rs35700518
SNPdbe	rs35700518
MSV3d	rs35700518
GWAS Ctlg	rs35700518

Max Magnitude

0

OMIM	142200
Desc
Variant	0006
Related	also

ClinVar
Risk	rs35700518(G;G)
Alt	rs35700518(G;G)
Reference	Rs35700518(T;T)
Significance	Other
Disease	HEMOGLOBIN F (COBB)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (COBB)
Reversed	1
HGVS	NC_000011.9:g.5270801A>C
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016150.1,

[PMID 2419280] Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly.