rs36104787

Orientation

plus

Stabilized

plus

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

Make rs36104787(C;G)

Make rs36104787(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177050

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs36104787
dbSNP (classic)	rs36104787
ClinGen	rs36104787
ebi	rs36104787
HLI	rs36104787
Exac	rs36104787
Gnomad	rs36104787
Varsome	rs36104787
LitVar	rs36104787
Map	rs36104787
PheGenI	rs36104787
Biobank	rs36104787
1000 genomes	rs36104787
hgdp	rs36104787
ensembl	rs36104787
geneview	rs36104787
scholar	rs36104787
google	rs36104787
pharmgkb	rs36104787
gwascentral	rs36104787
openSNP	rs36104787
23andMe	rs36104787
SNPshot	rs36104787
SNPdbe	rs36104787
MSV3d	rs36104787
GWAS Ctlg	rs36104787

Max Magnitude

0

OMIM	141800
Desc
Variant	0196
Related	also

OMIM	141850
Desc
Variant	0049
Related	also

ClinVar
Risk	rs36104787(G;G) rs36104787(T;T)
Alt	rs36104787(G;G) rs36104787(T;T)
Reference	Rs36104787(C;C)
Significance	Other
Disease	HEMOGLOBIN FUCHU-I
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN FUCHU-I
Reversed	0
HGVS	NC_000016.9:g.227049C>T
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000017215.2,

[PMID 8718697] Two new alpha chain variants: Hb Fuchu-I [alpha 72(EF1)His-->Tyr] and Hb Fuchu-II [alpha 97(G4)Asn-->His].