rs878853925
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(A;T) | 7.5 | Neurofibromatosis, type 2 |
Make rs878853925(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 29681491 |
Gene | NF2 |
is a | snp |
is | mentioned by |
dbSNP | rs878853925 |
dbSNP (classic) | rs878853925 |
ClinGen | rs878853925 |
ebi | rs878853925 |
HLI | rs878853925 |
Exac | rs878853925 |
Gnomad | rs878853925 |
Varsome | rs878853925 |
LitVar | rs878853925 |
Map | rs878853925 |
PheGenI | rs878853925 |
Biobank | rs878853925 |
1000 genomes | rs878853925 |
hgdp | rs878853925 |
ensembl | rs878853925 |
geneview | rs878853925 |
scholar | rs878853925 |
rs878853925 | |
pharmgkb | rs878853925 |
gwascentral | rs878853925 |
openSNP | rs878853925 |
23andMe | rs878853925 |
SNPshot | rs878853925 |
SNPdbe | rs878853925 |
MSV3d | rs878853925 |
GWAS Ctlg | rs878853925 |
Max Magnitude | 7.5 |
ClinVar | |
---|---|
Risk | rs878853925(T;T) |
Alt | rs878853925(T;T) |
Reference | Rs878853925(A;A) |
Significance | Pathogenic |
Disease | Neurofibromatosis |
Variation | info |
Gene | NF2 |
CLNDBN | Neurofibromatosis, type 2 |
Reversed | 0 |
HGVS | NC_000022.10:g.30077480A>T |
CLNSRC | |
CLNACC | RCV000232701.1, |