rs28931602
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs28931602(G;G) |
Make rs28931602(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 128335543 |
Gene | FBN2 |
is a | snp |
is | mentioned by |
dbSNP | rs28931602 |
dbSNP (classic) | rs28931602 |
ClinGen | rs28931602 |
ebi | rs28931602 |
HLI | rs28931602 |
Exac | rs28931602 |
Gnomad | rs28931602 |
Varsome | rs28931602 |
LitVar | rs28931602 |
Map | rs28931602 |
PheGenI | rs28931602 |
Biobank | rs28931602 |
1000 genomes | rs28931602 |
hgdp | rs28931602 |
ensembl | rs28931602 |
geneview | rs28931602 |
scholar | rs28931602 |
rs28931602 | |
pharmgkb | rs28931602 |
gwascentral | rs28931602 |
openSNP | rs28931602 |
23andMe | rs28931602 |
SNPshot | rs28931602 |
SNPdbe | rs28931602 |
MSV3d | rs28931602 |
GWAS Ctlg | rs28931602 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs28931602(G;G) |
Alt | rs28931602(G;G) |
Reference | Rs28931602(T;T) |
Significance | Pathogenic |
Disease | Congenital contractural arachnodactyly |
Variation | info |
Gene | FBN2 |
CLNDBN | Congenital contractural arachnodactyly |
Reversed | 1 |
HGVS | NC_000005.9:g.127671235A>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000000556.3, |