rs33970907

Orientation

minus

Stabilized

minus

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

Make rs33970907(A;G)

Make rs33970907(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249737

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs33970907
dbSNP (classic)	rs33970907
ClinGen	rs33970907
ebi	rs33970907
HLI	rs33970907
Exac	rs33970907
Gnomad	rs33970907
Varsome	rs33970907
LitVar	rs33970907
Map	rs33970907
PheGenI	rs33970907
Biobank	rs33970907
1000 genomes	rs33970907
hgdp	rs33970907
ensembl	rs33970907
geneview	rs33970907
scholar	rs33970907
google	rs33970907
pharmgkb	rs33970907
gwascentral	rs33970907
openSNP	rs33970907
23andMe	rs33970907
SNPshot	rs33970907
SNPdbe	rs33970907
MSV3d	rs33970907
GWAS Ctlg	rs33970907

Max Magnitude

0

OMIM	142200
Desc
Variant	0015
Related	also

OMIM	142250
Desc
Variant	0024
Related	also

OMIM	142250
Desc
Variant	0029
Related	also

ClinVar
Risk	rs33970907(G;G) rs33970907(T;T)
Alt	rs33970907(G;G) rs33970907(T;T)
Reference	Rs33970907(A;A)
Significance	Other
Disease	HEMOGLOBIN F (KUALA LUMPUR)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (KUALA LUMPUR)
Reversed	1
HGVS	NC_000011.9:g.5270967T>C
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016159.3,

[PMID 4765089] Structural identification of haemoglobin F Kuala Lumpur: alpha2 gamma2 22(B4)Asp leads to Gly; 136 Ala.