rs35431217

Orientation

plus

Stabilized

plus

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

Make rs35431217(A;C)

Make rs35431217(C;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173554

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs35431217
dbSNP (classic)	rs35431217
ClinGen	rs35431217
ebi	rs35431217
HLI	rs35431217
Exac	rs35431217
Gnomad	rs35431217
Varsome	rs35431217
LitVar	rs35431217
Map	rs35431217
PheGenI	rs35431217
Biobank	rs35431217
1000 genomes	rs35431217
hgdp	rs35431217
ensembl	rs35431217
geneview	rs35431217
scholar	rs35431217
google	rs35431217
pharmgkb	rs35431217
gwascentral	rs35431217
openSNP	rs35431217
23andMe	rs35431217
SNPshot	rs35431217
SNPdbe	rs35431217
MSV3d	rs35431217
GWAS Ctlg	rs35431217

Max Magnitude

0

OMIM	141800
Desc
Variant	0137
Related	also

ClinVar
Risk	rs35431217(C;C)
Alt	rs35431217(C;C)
Reference	Rs35431217(A;A)
Significance	Untested
Disease
Variation	info
Gene	HBA2
CLNDBN
Reversed	0
HGVS	NC_000016.9:g.223553A>C
CLNSRC
CLNACC

[PMID 4429670] Hemoglobin St. Claude or alpha2-127(H10)Lys leads to Thr-beta2.