rs752611838
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs752611838(A;A) |
Make rs752611838(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 63944804 |
Gene | SCN4A |
is a | snp |
is | mentioned by |
dbSNP | rs752611838 |
dbSNP (classic) | rs752611838 |
ClinGen | rs752611838 |
ebi | rs752611838 |
HLI | rs752611838 |
Exac | rs752611838 |
Gnomad | rs752611838 |
Varsome | rs752611838 |
LitVar | rs752611838 |
Map | rs752611838 |
PheGenI | rs752611838 |
Biobank | rs752611838 |
1000 genomes | rs752611838 |
hgdp | rs752611838 |
ensembl | rs752611838 |
geneview | rs752611838 |
scholar | rs752611838 |
rs752611838 | |
pharmgkb | rs752611838 |
gwascentral | rs752611838 |
openSNP | rs752611838 |
23andMe | rs752611838 |
SNPshot | rs752611838 |
SNPdbe | rs752611838 |
MSV3d | rs752611838 |
GWAS Ctlg | rs752611838 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752611838(A;A) |
Alt | rs752611838(A;A) |
Reference | Rs752611838(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN4A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.62022164C>A |
CLNSRC | |
CLNACC | RCV000493171.1, |