rs121918074

Orientation

plus

Stabilized

plus

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

Make rs121918074(A;A)

Make rs121918074(A;C)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31595247

Gene

TTR

is a	snp
is	mentioned by
dbSNP	rs121918074
dbSNP (classic)	rs121918074
ClinGen	rs121918074
ebi	rs121918074
HLI	rs121918074
Exac	rs121918074
Gnomad	rs121918074
Varsome	rs121918074
LitVar	rs121918074
Map	rs121918074
PheGenI	rs121918074
Biobank	rs121918074
1000 genomes	rs121918074
hgdp	rs121918074
ensembl	rs121918074
geneview	rs121918074
scholar	rs121918074
google	rs121918074
pharmgkb	rs121918074
gwascentral	rs121918074
openSNP	rs121918074
23andMe	rs121918074
SNPshot	rs121918074
SNPdbe	rs121918074
MSV3d	rs121918074
GWAS Ctlg	rs121918074

Max Magnitude

0

OMIM	176300
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121918074(A;A)
Alt	rs121918074(A;A)
Reference	Rs121918074(C;C)
Significance	Other
Disease	Amyloidogenic transthyretin amyloidosis not specified
Variation	info
Gene	TTR
CLNDBN	Amyloidogenic transthyretin amyloidosis not specified
Reversed	0
HGVS	NC_000018.9:g.29175210C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014369.27, RCV000152541.1,