rs34708054

Orientation

plus

Stabilized

plus

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

Make rs34708054(C;G)

Make rs34708054(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176777

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs34708054
dbSNP (classic)	rs34708054
ClinGen	rs34708054
ebi	rs34708054
HLI	rs34708054
Exac	rs34708054
Gnomad	rs34708054
Varsome	rs34708054
LitVar	rs34708054
Map	rs34708054
PheGenI	rs34708054
Biobank	rs34708054
1000 genomes	rs34708054
hgdp	rs34708054
ensembl	rs34708054
geneview	rs34708054
scholar	rs34708054
google	rs34708054
pharmgkb	rs34708054
gwascentral	rs34708054
openSNP	rs34708054
23andMe	rs34708054
SNPshot	rs34708054
SNPdbe	rs34708054
MSV3d	rs34708054
GWAS Ctlg	rs34708054

Max Magnitude

0

OMIM	141800
Desc
Variant	0104
Related	also

OMIM	141850
Desc
Variant	0042
Related	also

ClinVar
Risk	rs34708054(G;G) rs34708054(T;T)
Alt	rs34708054(G;G) rs34708054(T;T)
Reference	Rs34708054(C;C)
Significance	Other
Disease	HEMOGLOBIN NECKER ENFANTS-MALADES
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN NECKER ENFANTS-MALADES
Reversed	0
HGVS	NC_000016.9:g.226776C>T
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000017118.2,

[PMID 7390863] A silent hemoglobin variant: hemoglobin necker enfants-malades alpha 20 (B1) His leads to Tyr.