rs767569346
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs767569346(A;A) |
Make rs767569346(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 14158206 |
Gene | XPC |
is a | snp |
is | mentioned by |
dbSNP | rs767569346 |
dbSNP (classic) | rs767569346 |
ClinGen | rs767569346 |
ebi | rs767569346 |
HLI | rs767569346 |
Exac | rs767569346 |
Gnomad | rs767569346 |
Varsome | rs767569346 |
LitVar | rs767569346 |
Map | rs767569346 |
PheGenI | rs767569346 |
Biobank | rs767569346 |
1000 genomes | rs767569346 |
hgdp | rs767569346 |
ensembl | rs767569346 |
geneview | rs767569346 |
scholar | rs767569346 |
rs767569346 | |
pharmgkb | rs767569346 |
gwascentral | rs767569346 |
openSNP | rs767569346 |
23andMe | rs767569346 |
SNPshot | rs767569346 |
SNPdbe | rs767569346 |
MSV3d | rs767569346 |
GWAS Ctlg | rs767569346 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767569346(A;A) rs767569346(C;C) rs767569346(T;T) |
Alt | rs767569346(A;A) rs767569346(C;C) rs767569346(T;T) |
Reference | Rs767569346(G;G) |
Significance | Pathogenic |
Disease | Xeroderma pigmentosum |
Variation | info |
Gene | XPC |
CLNDBN | Xeroderma pigmentosum, group C |
Reversed | 0 |
HGVS | NC_000003.11:g.14199706G>T |
CLNSRC | |
CLNACC | RCV000170432.1, |