rs781626187
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs781626187(A;C) |
Make rs781626187(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 64016970 |
Gene | LOC105369801, SRGAP1 |
is a | snp |
is | mentioned by |
dbSNP | rs781626187 |
dbSNP (classic) | rs781626187 |
ClinGen | rs781626187 |
ebi | rs781626187 |
HLI | rs781626187 |
Exac | rs781626187 |
Gnomad | rs781626187 |
Varsome | rs781626187 |
LitVar | rs781626187 |
Map | rs781626187 |
PheGenI | rs781626187 |
Biobank | rs781626187 |
1000 genomes | rs781626187 |
hgdp | rs781626187 |
ensembl | rs781626187 |
geneview | rs781626187 |
scholar | rs781626187 |
rs781626187 | |
pharmgkb | rs781626187 |
gwascentral | rs781626187 |
openSNP | rs781626187 |
23andMe | rs781626187 |
SNPshot | rs781626187 |
SNPdbe | rs781626187 |
MSV3d | rs781626187 |
GWAS Ctlg | rs781626187 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs781626187(C;C) |
Alt | rs781626187(C;C) |
Reference | Rs781626187(A;A) |
Significance | Pathogenic |
Disease | Thyroid cancer |
Variation | info |
Gene | SRGAP1 |
CLNDBN | Thyroid cancer, follicular |
Reversed | 0 |
HGVS | NC_000012.11:g.64410750A>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000190471.2, |