rs71492753
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs71492753(-;-) |
Make rs71492753(-;GGCCCC) |
Make rs71492753(GGCCCC;GGCCCC) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 27573540 |
Gene | C9orf72 |
is a | snp |
is | mentioned by |
dbSNP | rs71492753 |
dbSNP (classic) | rs71492753 |
ClinGen | rs71492753 |
ebi | rs71492753 |
HLI | rs71492753 |
Exac | rs71492753 |
Gnomad | rs71492753 |
Varsome | rs71492753 |
LitVar | rs71492753 |
Map | rs71492753 |
PheGenI | rs71492753 |
Biobank | rs71492753 |
1000 genomes | rs71492753 |
hgdp | rs71492753 |
ensembl | rs71492753 |
geneview | rs71492753 |
scholar | rs71492753 |
rs71492753 | |
pharmgkb | rs71492753 |
gwascentral | rs71492753 |
openSNP | rs71492753 |
23andMe | rs71492753 |
SNPshot | rs71492753 |
SNPdbe | rs71492753 |
MSV3d | rs71492753 |
GWAS Ctlg | rs71492753 |
Max Magnitude | 0 |
aka NM_001256054.1(C9orf72):c.-45+163_-45+168GGGGCC[(24_?)]
OMIM pathogenic variant