rs121918089

Orientation

plus

Stabilized

plus

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

Make rs121918089(A;G)

Make rs121918089(G;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31598610

Gene

TTR

is a	snp
is	mentioned by
dbSNP	rs121918089
dbSNP (classic)	rs121918089
ClinGen	rs121918089
ebi	rs121918089
HLI	rs121918089
Exac	rs121918089
Gnomad	rs121918089
Varsome	rs121918089
LitVar	rs121918089
Map	rs121918089
PheGenI	rs121918089
Biobank	rs121918089
1000 genomes	rs121918089
hgdp	rs121918089
ensembl	rs121918089
geneview	rs121918089
scholar	rs121918089
google	rs121918089
pharmgkb	rs121918089
gwascentral	rs121918089
openSNP	rs121918089
23andMe	rs121918089
SNPshot	rs121918089
SNPdbe	rs121918089
MSV3d	rs121918089
GWAS Ctlg	rs121918089

Max Magnitude

0

OMIM	176300
Desc
Variant	0034
Related	also

ClinVar
Risk	rs121918089(G;G)
Alt	rs121918089(G;G)
Reference	Rs121918089(A;A)
Significance	Pathogenic
Disease	Amyloidogenic transthyretin amyloidosis
Variation	info
Gene	TTR
CLNDBN	Amyloidogenic transthyretin amyloidosis
Reversed	0
HGVS	NC_000018.9:g.29178573A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014392.17,