rs1085307459
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TCTC;TCTC) | 0 | common in clinvar |
Chromosome | 17 |
Position | 31325961 |
Gene | NF1 |
is a | snp |
is | mentioned by |
dbSNP | rs1085307459 |
dbSNP (classic) | rs1085307459 |
ClinGen | rs1085307459 |
ebi | rs1085307459 |
HLI | rs1085307459 |
Exac | rs1085307459 |
Gnomad | rs1085307459 |
Varsome | rs1085307459 |
LitVar | rs1085307459 |
Map | rs1085307459 |
PheGenI | rs1085307459 |
Biobank | rs1085307459 |
1000 genomes | rs1085307459 |
hgdp | rs1085307459 |
ensembl | rs1085307459 |
geneview | rs1085307459 |
scholar | rs1085307459 |
rs1085307459 | |
pharmgkb | rs1085307459 |
gwascentral | rs1085307459 |
openSNP | rs1085307459 |
23andMe | rs1085307459 |
SNPshot | rs1085307459 |
SNPdbe | rs1085307459 |
MSV3d | rs1085307459 |
GWAS Ctlg | rs1085307459 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1085307459(-;-) |
Alt | rs1085307459(-;-) |
Reference | Rs1085307459(TCTC;TCTC) |
Significance | Pathogenic |
Disease | not provided Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | NF1 |
CLNDBN | not provided Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000017.10:g.29652979_29652982delCTCT |
CLNSRC | |
CLNACC | RCV000489809.1, RCV000492080.1, |