rs34472107

Orientation

plus

Stabilized

plus

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

Make rs34472107(C;T)

Make rs34472107(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177325

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs34472107
dbSNP (classic)	rs34472107
ClinGen	rs34472107
ebi	rs34472107
HLI	rs34472107
Exac	rs34472107
Gnomad	rs34472107
Varsome	rs34472107
LitVar	rs34472107
Map	rs34472107
PheGenI	rs34472107
Biobank	rs34472107
1000 genomes	rs34472107
hgdp	rs34472107
ensembl	rs34472107
geneview	rs34472107
scholar	rs34472107
google	rs34472107
pharmgkb	rs34472107
gwascentral	rs34472107
openSNP	rs34472107
23andMe	rs34472107
SNPshot	rs34472107
SNPdbe	rs34472107
MSV3d	rs34472107
GWAS Ctlg	rs34472107

Merged from

Rs63751114

Max Magnitude

0

OMIM	141800
Desc
Variant	0183
Related	also

ClinVar
Risk	rs34472107(G;G) rs34472107(T;T)
Alt	rs34472107(G;G) rs34472107(T;T)
Reference	Rs34472107(C;C)
Significance	Other
Disease	HEMOGLOBIN MELUSINE
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN MELUSINE
Reversed	0
HGVS	NC_000016.9:g.227324C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017203.2,

[PMID 8294199] Hb Melusine [alpha 114(GH2)Pro-->Ser]: a new neutral hemoglobin variant.