rs77969175
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common/normal |
(G;T) | 3 | carrier of a spinal muscular atrophy disease allele |
Make rs77969175(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 70951941 |
Gene | SMN1 |
is a | snp |
is | mentioned by |
dbSNP | rs77969175 |
dbSNP (classic) | rs77969175 |
ClinGen | rs77969175 |
ebi | rs77969175 |
HLI | rs77969175 |
Exac | rs77969175 |
Gnomad | rs77969175 |
Varsome | rs77969175 |
LitVar | rs77969175 |
Map | rs77969175 |
PheGenI | rs77969175 |
Biobank | rs77969175 |
1000 genomes | rs77969175 |
hgdp | rs77969175 |
ensembl | rs77969175 |
geneview | rs77969175 |
scholar | rs77969175 |
rs77969175 | |
pharmgkb | rs77969175 |
gwascentral | rs77969175 |
openSNP | rs77969175 |
23andMe | rs77969175 |
SNPshot | rs77969175 |
SNPdbe | rs77969175 |
MSV3d | rs77969175 |
GWAS Ctlg | rs77969175 |
Max Magnitude | 3 |