rs58640772
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs58640772(-;-) |
Make rs58640772(-;GCGCTACGTGGAG) |
Make rs58640772(GCGCTACGTGGAG;GCGCTACGTGGAG) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 8 |
Position | 24956455 |
Gene | NEFL |
is a | snp |
is | mentioned by |
dbSNP | rs58640772 |
dbSNP (classic) | rs58640772 |
ClinGen | rs58640772 |
ebi | rs58640772 |
HLI | rs58640772 |
Exac | rs58640772 |
Gnomad | rs58640772 |
Varsome | rs58640772 |
LitVar | rs58640772 |
Map | rs58640772 |
PheGenI | rs58640772 |
Biobank | rs58640772 |
1000 genomes | rs58640772 |
hgdp | rs58640772 |
ensembl | rs58640772 |
geneview | rs58640772 |
scholar | rs58640772 |
rs58640772 | |
pharmgkb | rs58640772 |
gwascentral | rs58640772 |
openSNP | rs58640772 |
23andMe | rs58640772 |
SNPshot | rs58640772 |
SNPdbe | rs58640772 |
MSV3d | rs58640772 |
GWAS Ctlg | rs58640772 |
Max Magnitude | 0 |
aka NM_006158.4(NEFL):c.48_60dupGCGCTACGTGGAG or (p.Thr21Alafs)
OMIM pathogenic variant