rs121913128

Orientation

plus

Stabilized

plus

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

Make rs121913128(-;-)

Make rs121913128(-;CGT)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177406

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs121913128
dbSNP (classic)	rs121913128
ClinGen	rs121913128
ebi	rs121913128
HLI	rs121913128
Exac	rs121913128
Gnomad	rs121913128
Varsome	rs121913128
LitVar	rs121913128
Map	rs121913128
PheGenI	rs121913128
Biobank	rs121913128
1000 genomes	rs121913128
hgdp	rs121913128
ensembl	rs121913128
geneview	rs121913128
scholar	rs121913128
google	rs121913128
pharmgkb	rs121913128
gwascentral	rs121913128
openSNP	rs121913128
23andMe	rs121913128
SNPshot	rs121913128
SNPdbe	rs121913128
MSV3d	rs121913128
GWAS Ctlg	rs121913128

Max Magnitude

0

OMIM	141800
Desc
Variant	0083
Related	also

ClinVar
Risk	rs121913128(-;-)
Alt	rs121913128(-;-)
Reference	Rs121913128(CGT;CGT)
Significance	Other
Disease	HEMOGLOBIN KOELLIKER HEMOGLOBIN F (KOELLIKER)
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN KOELLIKER HEMOGLOBIN F (KOELLIKER)
Reversed	0
HGVS	NC_000016.9:g.227405_227407delCGT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017081.3, RCV000017082.3,