rs387906320
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier of a sclerosteosis type 1 mutation |
Make rs387906320(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 43758672 |
Gene | SOST |
is a | snp |
is | mentioned by |
dbSNP | rs387906320 |
dbSNP (classic) | rs387906320 |
ClinGen | rs387906320 |
ebi | rs387906320 |
HLI | rs387906320 |
Exac | rs387906320 |
Gnomad | rs387906320 |
Varsome | rs387906320 |
LitVar | rs387906320 |
Map | rs387906320 |
PheGenI | rs387906320 |
Biobank | rs387906320 |
1000 genomes | rs387906320 |
hgdp | rs387906320 |
ensembl | rs387906320 |
geneview | rs387906320 |
scholar | rs387906320 |
rs387906320 | |
pharmgkb | rs387906320 |
gwascentral | rs387906320 |
openSNP | rs387906320 |
23andMe | rs387906320 |
SNPshot | rs387906320 |
SNPdbe | rs387906320 |
MSV3d | rs387906320 |
GWAS Ctlg | rs387906320 |
Max Magnitude | 3 |
aka c.70C>T (p.Gln24Ter)
ClinVar | |
---|---|
Risk | rs387906320(T;T) |
Alt | rs387906320(T;T) |
Reference | Rs387906320(C;C) |
Significance | Pathogenic |
Disease | Sclerosteosis |
Variation | info |
Gene | SOST |
CLNDBN | Sclerosteosis |
Reversed | 1 |
HGVS | NC_000017.10:g.41836040G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005049.3, |