rs121918095

Orientation

plus

Stabilized

plus

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

Make rs121918095(A;A)

Make rs121918095(A;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31598602

Gene

TTR

is a	snp
is	mentioned by
dbSNP	rs121918095
dbSNP (classic)	rs121918095
ClinGen	rs121918095
ebi	rs121918095
HLI	rs121918095
Exac	rs121918095
Gnomad	rs121918095
Varsome	rs121918095
LitVar	rs121918095
Map	rs121918095
PheGenI	rs121918095
Biobank	rs121918095
1000 genomes	rs121918095
hgdp	rs121918095
ensembl	rs121918095
geneview	rs121918095
scholar	rs121918095
google	rs121918095
pharmgkb	rs121918095
gwascentral	rs121918095
openSNP	rs121918095
23andMe	rs121918095
SNPshot	rs121918095
SNPdbe	rs121918095
MSV3d	rs121918095
GWAS Ctlg	rs121918095

GMAF

0.003673

Max Magnitude

0

OMIM	176300
Desc
Variant	0042
Related	also

ClinVar
Risk	rs121918095(A;A)
Alt	rs121918095(A;A)
Reference	Rs121918095(G;G)
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.29178565G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014400.28, RCV000152543.1,