rs1064795730
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TATCCAATGC;TATCCAATGC) | 0 | common in clinvar |
Chromosome | 17 |
Position | 31229406 |
Gene | NF1 |
is a | snp |
is | mentioned by |
dbSNP | rs1064795730 |
dbSNP (old) | rs1064795730 |
ClinGen | rs1064795730 |
ebi | rs1064795730 |
HLI | rs1064795730 |
Exac | rs1064795730 |
Gnomad | rs1064795730 |
Varsome | rs1064795730 |
Map | rs1064795730 |
PheGenI | rs1064795730 |
Biobank | rs1064795730 |
1000 genomes | rs1064795730 |
hgdp | rs1064795730 |
ensembl | rs1064795730 |
gopubmed | rs1064795730 |
geneview | rs1064795730 |
scholar | rs1064795730 |
rs1064795730 | |
pharmgkb | rs1064795730 |
gwascentral | rs1064795730 |
openSNP | rs1064795730 |
23andMe | rs1064795730 |
23andMe all | rs1064795730 |
SNPshot | rs1064795730 |
SNPdbe | rs1064795730 |
MSV3d | rs1064795730 |
GWAS Ctlg | rs1064795730 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064795730(-;-) |
Alt | rs1064795730(-;-) |
Reference | Rs1064795730(TATCCAATGC;TATCCAATGC) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | NF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.29556424_29556433delCCAATGCTAT |
CLNSRC | |
CLNACC | RCV000485560.1, |