rs7297245
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(T;T) | 0 | common on affy axiom data |
Make rs7297245(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 95980836 |
Gene | HAL |
is a | snp |
is | mentioned by |
dbSNP | rs7297245 |
dbSNP (classic) | rs7297245 |
ClinGen | rs7297245 |
ebi | rs7297245 |
HLI | rs7297245 |
Exac | rs7297245 |
Gnomad | rs7297245 |
Varsome | rs7297245 |
LitVar | rs7297245 |
Map | rs7297245 |
PheGenI | rs7297245 |
Biobank | rs7297245 |
1000 genomes | rs7297245 |
hgdp | rs7297245 |
ensembl | rs7297245 |
geneview | rs7297245 |
scholar | rs7297245 |
rs7297245 | |
pharmgkb | rs7297245 |
gwascentral | rs7297245 |
openSNP | rs7297245 |
23andMe | rs7297245 |
SNPshot | rs7297245 |
SNPdbe | rs7297245 |
MSV3d | rs7297245 |
GWAS Ctlg | rs7297245 |
GMAF | 0.1093 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 18641401] A role for ultraviolet radiation immunosuppression in non-melanoma skin cancer as evidenced by gene-environment interactions.
[PMID 18853455] Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.
ClinVar | |
---|---|
Risk | Rs7297245(T;T) |
Alt | Rs7297245(T;T) |
Reference | Rs7297245(C;C) |
Significance | Non-pathogenic |
Disease | Histidinemia |
Variation | info |
Gene | HAL |
CLNDBN | Histidinemia |
Reversed | 0 |
HGVS | NC_000012.11:g.96374614C>T |
CLNSRC | |
CLNACC | RCV000385709.1, |