rs879255545
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs879255545(-;CCTGGAGCCCGTAT) |
Make rs879255545(CCTGGAGCCCGTAT;CCTGGAGCCCGTAT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 68829868 |
Gene | EFNB1 |
is a | snp |
is | mentioned by |
dbSNP | rs879255545 |
dbSNP (classic) | rs879255545 |
ClinGen | rs879255545 |
ebi | rs879255545 |
HLI | rs879255545 |
Exac | rs879255545 |
Gnomad | rs879255545 |
Varsome | rs879255545 |
LitVar | rs879255545 |
Map | rs879255545 |
PheGenI | rs879255545 |
Biobank | rs879255545 |
1000 genomes | rs879255545 |
hgdp | rs879255545 |
ensembl | rs879255545 |
geneview | rs879255545 |
scholar | rs879255545 |
rs879255545 | |
pharmgkb | rs879255545 |
gwascentral | rs879255545 |
openSNP | rs879255545 |
23andMe | rs879255545 |
SNPshot | rs879255545 |
SNPdbe | rs879255545 |
MSV3d | rs879255545 |
GWAS Ctlg | rs879255545 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255545(CCTGGAGCCCGTAT;CCTGGAGCCCGTAT) |
Alt | rs879255545(CCTGGAGCCCGTAT;CCTGGAGCCCGTAT) |
Reference | Rs879255545(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | EFNB1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.68049711_68049712insCCTGGAGCCCGTAT |
CLNSRC | |
CLNACC | RCV000224501.1, |