rs121918087

Orientation

plus

Stabilized

plus

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

Make rs121918087(C;G)

Make rs121918087(G;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31598581

Gene

TTR

is a	snp
is	mentioned by
dbSNP	rs121918087
dbSNP (classic)	rs121918087
ClinGen	rs121918087
ebi	rs121918087
HLI	rs121918087
Exac	rs121918087
Gnomad	rs121918087
Varsome	rs121918087
LitVar	rs121918087
Map	rs121918087
PheGenI	rs121918087
Biobank	rs121918087
1000 genomes	rs121918087
hgdp	rs121918087
ensembl	rs121918087
geneview	rs121918087
scholar	rs121918087
google	rs121918087
pharmgkb	rs121918087
gwascentral	rs121918087
openSNP	rs121918087
23andMe	rs121918087
SNPshot	rs121918087
SNPdbe	rs121918087
MSV3d	rs121918087
GWAS Ctlg	rs121918087

Max Magnitude

0

OMIM	176300
Desc
Variant	0032
Related	also

ClinVar
Risk	rs121918087(G;G)
Alt	rs121918087(G;G)
Reference	Rs121918087(C;C)
Significance	Pathogenic
Disease	Amyloidogenic transthyretin amyloidosis
Variation	info
Gene	TTR
CLNDBN	Amyloidogenic transthyretin amyloidosis
Reversed	0
HGVS	NC_000018.9:g.29178544C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014390.24,