rs137853214
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs137853214(G;T) |
Make rs137853214(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 87349304 |
Gene | CCNH, RASA1 |
is a | snp |
is | mentioned by |
dbSNP | rs137853214 |
dbSNP (classic) | rs137853214 |
ClinGen | rs137853214 |
ebi | rs137853214 |
HLI | rs137853214 |
Exac | rs137853214 |
Gnomad | rs137853214 |
Varsome | rs137853214 |
LitVar | rs137853214 |
Map | rs137853214 |
PheGenI | rs137853214 |
Biobank | rs137853214 |
1000 genomes | rs137853214 |
hgdp | rs137853214 |
ensembl | rs137853214 |
geneview | rs137853214 |
scholar | rs137853214 |
rs137853214 | |
pharmgkb | rs137853214 |
gwascentral | rs137853214 |
openSNP | rs137853214 |
23andMe | rs137853214 |
SNPshot | rs137853214 |
SNPdbe | rs137853214 |
MSV3d | rs137853214 |
GWAS Ctlg | rs137853214 |
Merged from | Rs28932771 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853214(T;T) |
Alt | rs137853214(T;T) |
Reference | Rs137853214(G;G) |
Significance | Pathogenic |
Disease | Basal cell carcinoma |
Variation | info |
Gene | RASA1 |
CLNDBN | Basal cell carcinoma, somatic |
Reversed | 0 |
HGVS | NC_000005.9:g.86645121G>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017367.4, |