rs121918100

Orientation

plus

Stabilized

plus

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

Make rs121918100(C;C)

Make rs121918100(C;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31595184

Gene

TTR

is a	snp
is	mentioned by
dbSNP	rs121918100
dbSNP (classic)	rs121918100
ClinGen	rs121918100
ebi	rs121918100
HLI	rs121918100
Exac	rs121918100
Gnomad	rs121918100
Varsome	rs121918100
LitVar	rs121918100
Map	rs121918100
PheGenI	rs121918100
Biobank	rs121918100
1000 genomes	rs121918100
hgdp	rs121918100
ensembl	rs121918100
geneview	rs121918100
scholar	rs121918100
google	rs121918100
pharmgkb	rs121918100
gwascentral	rs121918100
openSNP	rs121918100
23andMe	rs121918100
SNPshot	rs121918100
SNPdbe	rs121918100
MSV3d	rs121918100
GWAS Ctlg	rs121918100

Max Magnitude

0

OMIM	176300
Desc
Variant	0050
Related	also

ClinVar
Risk	rs121918100(C;C)
Alt	rs121918100(C;C)
Reference	Rs121918100(T;T)
Significance	Pathogenic
Disease	AMYLOIDOSIS
Variation	info
Gene	TTR
CLNDBN	AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
Reversed	0
HGVS	NC_000018.9:g.29175147T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014408.24,