rs1064796486
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Chromosome | 2 |
Position | 218662628 |
Gene | BCS1L |
is a | snp |
is | mentioned by |
dbSNP | rs1064796486 |
dbSNP (classic) | rs1064796486 |
ClinGen | rs1064796486 |
ebi | rs1064796486 |
HLI | rs1064796486 |
Exac | rs1064796486 |
Gnomad | rs1064796486 |
Varsome | rs1064796486 |
LitVar | rs1064796486 |
Map | rs1064796486 |
PheGenI | rs1064796486 |
Biobank | rs1064796486 |
1000 genomes | rs1064796486 |
hgdp | rs1064796486 |
ensembl | rs1064796486 |
geneview | rs1064796486 |
scholar | rs1064796486 |
rs1064796486 | |
pharmgkb | rs1064796486 |
gwascentral | rs1064796486 |
openSNP | rs1064796486 |
23andMe | rs1064796486 |
SNPshot | rs1064796486 |
SNPdbe | rs1064796486 |
MSV3d | rs1064796486 |
GWAS Ctlg | rs1064796486 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064796486(T;T) |
Alt | rs1064796486(T;T) |
Reference | Rs1064796486(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | BCS1L |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.219527351C>T |
CLNSRC | |
CLNACC | RCV000480400.1, |