rs150140314
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs150140314(C;T) |
Make rs150140314(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 157133100 |
Gene | ARID1B |
is a | snp |
is | mentioned by |
dbSNP | rs150140314 |
dbSNP (classic) | rs150140314 |
ClinGen | rs150140314 |
ebi | rs150140314 |
HLI | rs150140314 |
Exac | rs150140314 |
Gnomad | rs150140314 |
Varsome | rs150140314 |
LitVar | rs150140314 |
Map | rs150140314 |
PheGenI | rs150140314 |
Biobank | rs150140314 |
1000 genomes | rs150140314 |
hgdp | rs150140314 |
ensembl | rs150140314 |
geneview | rs150140314 |
scholar | rs150140314 |
rs150140314 | |
pharmgkb | rs150140314 |
gwascentral | rs150140314 |
openSNP | rs150140314 |
23andMe | rs150140314 |
SNPshot | rs150140314 |
SNPdbe | rs150140314 |
MSV3d | rs150140314 |
GWAS Ctlg | rs150140314 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs150140314(T;T) |
Alt | rs150140314(T;T) |
Reference | Rs150140314(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | ARID1B |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000006.11:g.157454234C>T |
CLNSRC | |
CLNACC | RCV000171403.2, |