rs36038739

Orientation

minus

Stabilized

minus

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

Make rs36038739(G;T)

Make rs36038739(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226604

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs36038739
dbSNP (classic)	rs36038739
ClinGen	rs36038739
ebi	rs36038739
HLI	rs36038739
Exac	rs36038739
Gnomad	rs36038739
Varsome	rs36038739
LitVar	rs36038739
Map	rs36038739
PheGenI	rs36038739
Biobank	rs36038739
1000 genomes	rs36038739
hgdp	rs36038739
ensembl	rs36038739
geneview	rs36038739
scholar	rs36038739
google	rs36038739
pharmgkb	rs36038739
gwascentral	rs36038739
openSNP	rs36038739
23andMe	rs36038739
SNPshot	rs36038739
SNPdbe	rs36038739
MSV3d	rs36038739
GWAS Ctlg	rs36038739

Max Magnitude

0

OMIM	141900
Desc
Variant	0067
Related	also

ClinVar
Risk	rs36038739(A;A) rs36038739(C;C) rs36038739(T;T)
Alt	rs36038739(A;A) rs36038739(C;C) rs36038739(T;T)
Reference	Rs36038739(G;G)
Significance	Other
Disease	HEMOGLOBIN DETROIT not specified
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN DETROIT not specified
Reversed	1
HGVS	NC_000011.9:g.5247834C>G; NC_000011.9:g.5247834C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016325.3, RCV000244119.1,

[PMID 708768] Hemoglobin Detroit: beta95 (FG2) lysine leads to asparagine.