rs121918078

Orientation

plus

Stabilized

plus

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

Make rs121918078(A;A)

Make rs121918078(A;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31593019

Gene

TTR

is a	snp
is	mentioned by
dbSNP	rs121918078
dbSNP (classic)	rs121918078
ClinGen	rs121918078
ebi	rs121918078
HLI	rs121918078
Exac	rs121918078
Gnomad	rs121918078
Varsome	rs121918078
LitVar	rs121918078
Map	rs121918078
PheGenI	rs121918078
Biobank	rs121918078
1000 genomes	rs121918078
hgdp	rs121918078
ensembl	rs121918078
geneview	rs121918078
scholar	rs121918078
google	rs121918078
pharmgkb	rs121918078
gwascentral	rs121918078
openSNP	rs121918078
23andMe	rs121918078
SNPshot	rs121918078
SNPdbe	rs121918078
MSV3d	rs121918078
GWAS Ctlg	rs121918078

Max Magnitude

0

OMIM	176300
Desc
Variant	0021
Related	also

ClinVar
Risk	rs121918078(A;A)
Alt	rs121918078(A;A)
Reference	Rs121918078(G;G)
Significance	Untested
Disease	Amyloidogenic transthyretin amyloidosis
Variation	info
Gene	TTR
CLNDBN	Amyloidogenic transthyretin amyloidosis
Reversed	0
HGVS	NC_000018.9:g.29172982G>A
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000034628.1, SCV000034628.1,