rs28933981

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs28933981(C;T)

Make rs28933981(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31598647

Gene

TTR

is a	snp
is	mentioned by
dbSNP	rs28933981
dbSNP (classic)	rs28933981
ClinGen	rs28933981
ebi	rs28933981
HLI	rs28933981
Exac	rs28933981
Gnomad	rs28933981
Varsome	rs28933981
LitVar	rs28933981
Map	rs28933981
PheGenI	rs28933981
Biobank	rs28933981
1000 genomes	rs28933981
hgdp	rs28933981
ensembl	rs28933981
geneview	rs28933981
scholar	rs28933981
google	rs28933981
pharmgkb	rs28933981
gwascentral	rs28933981
openSNP	rs28933981
23andMe	rs28933981
SNPshot	rs28933981
SNPdbe	rs28933981
MSV3d	rs28933981
GWAS Ctlg	rs28933981

GMAF

0.001837

Max Magnitude

0

OMIM	176300
Desc	PREALBUMIN CHICAGO
Variant	0018
Related	also

ClinVar
Risk	rs28933981(T;T)
Alt	rs28933981(T;T)
Reference	Rs28933981(C;C)
Significance	Other
Disease	AMYLOIDOSIS not specified Amyloidogenic transthyretin amyloidosis
Variation	info
Gene	TTR
CLNDBN	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED, MODIFIER OF not specified Amyloidogenic transthyretin amyloidosis
Reversed	0
HGVS	NC_000018.9:g.29178610C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014376.18, RCV000036376.3, RCV000475117.1,