rs606231215

Merged into

rs34224604

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs606231215(-;-)

Make rs606231215(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

5234127

Gene

HBD

is a	snp
is	mentioned by
dbSNP	rs606231215
dbSNP (classic)	rs606231215
ClinGen	rs606231215
ebi	rs606231215
HLI	rs606231215
Exac	rs606231215
Gnomad	rs606231215
Varsome	rs606231215
LitVar	rs606231215
Map	rs606231215
PheGenI	rs606231215
Biobank	rs606231215
1000 genomes	rs606231215
hgdp	rs606231215
ensembl	rs606231215
geneview	rs606231215
scholar	rs606231215
google	rs606231215
pharmgkb	rs606231215
gwascentral	rs606231215
openSNP	rs606231215
23andMe	rs606231215
SNPshot	rs606231215
SNPdbe	rs606231215
MSV3d	rs606231215
GWAS Ctlg	rs606231215

Status

Merged into rs34224604

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs606231215(A;A)
Significance	Pathogenic
Disease	Delta-zero-thalassemia
Variation	info
Gene	HBD
CLNDBN	Delta-zero-thalassemia, knossos type
Reversed	1
HGVS	NC_000011.9:g.5255357delT
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016215.25,