rs772398324
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs772398324(-;-) |
Make rs772398324(-;T) |
Make rs772398324(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 15 |
Position | 48136733 |
Gene | MYEF2, SLC24A5 |
is a | snp |
is | mentioned by |
dbSNP | rs772398324 |
dbSNP (classic) | rs772398324 |
ClinGen | rs772398324 |
ebi | rs772398324 |
HLI | rs772398324 |
Exac | rs772398324 |
Gnomad | rs772398324 |
Varsome | rs772398324 |
LitVar | rs772398324 |
Map | rs772398324 |
PheGenI | rs772398324 |
Biobank | rs772398324 |
1000 genomes | rs772398324 |
hgdp | rs772398324 |
ensembl | rs772398324 |
geneview | rs772398324 |
scholar | rs772398324 |
rs772398324 | |
pharmgkb | rs772398324 |
gwascentral | rs772398324 |
openSNP | rs772398324 |
23andMe | rs772398324 |
SNPshot | rs772398324 |
SNPdbe | rs772398324 |
MSV3d | rs772398324 |
GWAS Ctlg | rs772398324 |
Max Magnitude | 0 |
aka NM_205850.2(SLC24A5):c.641delT or (p.Leu214Argfs)
OMIM pathogenic variant