rs35816645

Orientation

plus

Stabilized

plus

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

Make rs35816645(C;C)

Make rs35816645(C;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176762

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs35816645
dbSNP (classic)	rs35816645
ClinGen	rs35816645
ebi	rs35816645
HLI	rs35816645
Exac	rs35816645
Gnomad	rs35816645
Varsome	rs35816645
LitVar	rs35816645
Map	rs35816645
PheGenI	rs35816645
Biobank	rs35816645
1000 genomes	rs35816645
hgdp	rs35816645
ensembl	rs35816645
geneview	rs35816645
scholar	rs35816645
google	rs35816645
pharmgkb	rs35816645
gwascentral	rs35816645
openSNP	rs35816645
23andMe	rs35816645
SNPshot	rs35816645
SNPdbe	rs35816645
MSV3d	rs35816645
GWAS Ctlg	rs35816645

Max Magnitude

0

OMIM	141800
Desc
Variant	0114
Related	also

ClinVar
Risk	rs35816645(C;C) rs35816645(T;T)
Alt	rs35816645(C;C) rs35816645(T;T)
Reference	Rs35816645(G;G)
Significance	Other
Disease	HEMOGLOBIN OTTAWA HEMOGLOBIN SIAM
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN OTTAWA HEMOGLOBIN SIAM
Reversed	0
HGVS	NC_000016.9:g.226761G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017136.2, RCV000017137.2,

[PMID 4135957] Hemoglobin Siam (alpha 2 15 arg beta 2): a new alpha-chain variant.

[PMID 11939517] Hb Siam [alpha15(A13)Gly-->Arg (alpha1) (GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect.