rs201269335
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs201269335(A;T) |
Make rs201269335(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 148101440 |
Gene | SPINK5 |
is a | snp |
is | mentioned by |
dbSNP | rs201269335 |
dbSNP (classic) | rs201269335 |
ClinGen | rs201269335 |
ebi | rs201269335 |
HLI | rs201269335 |
Exac | rs201269335 |
Gnomad | rs201269335 |
Varsome | rs201269335 |
LitVar | rs201269335 |
Map | rs201269335 |
PheGenI | rs201269335 |
Biobank | rs201269335 |
1000 genomes | rs201269335 |
hgdp | rs201269335 |
ensembl | rs201269335 |
geneview | rs201269335 |
scholar | rs201269335 |
rs201269335 | |
pharmgkb | rs201269335 |
gwascentral | rs201269335 |
openSNP | rs201269335 |
23andMe | rs201269335 |
SNPshot | rs201269335 |
SNPdbe | rs201269335 |
MSV3d | rs201269335 |
GWAS Ctlg | rs201269335 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201269335(T;T) |
Alt | rs201269335(T;T) |
Reference | Rs201269335(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SPINK5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.147481003A>T |
CLNSRC | |
CLNACC | RCV000344894.1, |