rs763608512
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs763608512(A;A) |
Make rs763608512(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 52519825 |
Gene | KRT5 |
is a | snp |
is | mentioned by |
dbSNP | rs763608512 |
dbSNP (classic) | rs763608512 |
ClinGen | rs763608512 |
ebi | rs763608512 |
HLI | rs763608512 |
Exac | rs763608512 |
Gnomad | rs763608512 |
Varsome | rs763608512 |
LitVar | rs763608512 |
Map | rs763608512 |
PheGenI | rs763608512 |
Biobank | rs763608512 |
1000 genomes | rs763608512 |
hgdp | rs763608512 |
ensembl | rs763608512 |
geneview | rs763608512 |
scholar | rs763608512 |
rs763608512 | |
pharmgkb | rs763608512 |
gwascentral | rs763608512 |
openSNP | rs763608512 |
23andMe | rs763608512 |
SNPshot | rs763608512 |
SNPdbe | rs763608512 |
MSV3d | rs763608512 |
GWAS Ctlg | rs763608512 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763608512(A;A) rs763608512(T;T) |
Alt | rs763608512(A;A) rs763608512(T;T) |
Reference | Rs763608512(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KRT5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.52913609C>A |
CLNSRC | |
CLNACC | RCV000435783.1, |