rs759607901
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs759607901(C;T) |
Make rs759607901(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 43604637 |
Gene | POLH |
is a | snp |
is | mentioned by |
dbSNP | rs759607901 |
dbSNP (classic) | rs759607901 |
ClinGen | rs759607901 |
ebi | rs759607901 |
HLI | rs759607901 |
Exac | rs759607901 |
Gnomad | rs759607901 |
Varsome | rs759607901 |
LitVar | rs759607901 |
Map | rs759607901 |
PheGenI | rs759607901 |
Biobank | rs759607901 |
1000 genomes | rs759607901 |
hgdp | rs759607901 |
ensembl | rs759607901 |
geneview | rs759607901 |
scholar | rs759607901 |
rs759607901 | |
pharmgkb | rs759607901 |
gwascentral | rs759607901 |
openSNP | rs759607901 |
23andMe | rs759607901 |
SNPshot | rs759607901 |
SNPdbe | rs759607901 |
MSV3d | rs759607901 |
GWAS Ctlg | rs759607901 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759607901(T;T) |
Alt | rs759607901(T;T) |
Reference | Rs759607901(C;C) |
Significance | Pathogenic |
Disease | Xeroderma pigmentosum |
Variation | info |
Gene | POLH |
CLNDBN | Xeroderma pigmentosum, variant type |
Reversed | 0 |
HGVS | NC_000006.11:g.43572374C>T |
CLNSRC | |
CLNACC | RCV000209179.1, |