rs121918096
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;GTC) | 5.5 | TTR-related amyloidosis |
(GTC;GTC) | 0 | common in clinvar |
Make rs121918096(-;-) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 31598655 |
Gene | TTR |
is a | snp |
is | mentioned by |
dbSNP | rs121918096 |
dbSNP (classic) | rs121918096 |
ClinGen | rs121918096 |
ebi | rs121918096 |
HLI | rs121918096 |
Exac | rs121918096 |
Gnomad | rs121918096 |
Varsome | rs121918096 |
LitVar | rs121918096 |
Map | rs121918096 |
PheGenI | rs121918096 |
Biobank | rs121918096 |
1000 genomes | rs121918096 |
hgdp | rs121918096 |
ensembl | rs121918096 |
geneview | rs121918096 |
scholar | rs121918096 |
rs121918096 | |
pharmgkb | rs121918096 |
gwascentral | rs121918096 |
openSNP | rs121918096 |
23andMe | rs121918096 |
SNPshot | rs121918096 |
SNPdbe | rs121918096 |
MSV3d | rs121918096 |
GWAS Ctlg | rs121918096 |
Max Magnitude | 5.5 |
ClinVar | |
---|---|
Risk | rs121918096(-;-) |
Alt | rs121918096(-;-) |
Reference | Rs121918096(GTC;GTC) |
Significance | Other |
Disease | Amyloidogenic transthyretin amyloidosis |
Variation | info |
Gene | TTR |
CLNDBN | Amyloidogenic transthyretin amyloidosis |
Reversed | 0 |
HGVS | NC_000018.9:g.29178618_29178620delGTC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014402.28, |