rs267607281
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs267607281(A;A) |
Make rs267607281(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 102846349 |
Gene | BIVM-ERCC5, ERCC5 |
is a | snp |
is | mentioned by |
dbSNP | rs267607281 |
dbSNP (classic) | rs267607281 |
ClinGen | rs267607281 |
ebi | rs267607281 |
HLI | rs267607281 |
Exac | rs267607281 |
Gnomad | rs267607281 |
Varsome | rs267607281 |
LitVar | rs267607281 |
Map | rs267607281 |
PheGenI | rs267607281 |
Biobank | rs267607281 |
1000 genomes | rs267607281 |
hgdp | rs267607281 |
ensembl | rs267607281 |
geneview | rs267607281 |
scholar | rs267607281 |
rs267607281 | |
pharmgkb | rs267607281 |
gwascentral | rs267607281 |
openSNP | rs267607281 |
23andMe | rs267607281 |
SNPshot | rs267607281 |
SNPdbe | rs267607281 |
MSV3d | rs267607281 |
GWAS Ctlg | rs267607281 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267607281(A;A) |
Alt | rs267607281(A;A) |
Reference | Rs267607281(C;C) |
Significance | Pathogenic |
Disease | Xeroderma pigmentosum |
Variation | info |
Gene | BIVM-ERCC5 ERCC5 |
CLNDBN | Xeroderma pigmentosum, group G |
Reversed | 0 |
HGVS | NC_000013.10:g.103498699C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000034376.26, |