rs77672568
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs77672568(-;G) |
Make rs77672568(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 12807213 |
Gene | RNASEH2A |
is a | snp |
is | mentioned by |
dbSNP | rs77672568 |
dbSNP (classic) | rs77672568 |
ClinGen | rs77672568 |
ebi | rs77672568 |
HLI | rs77672568 |
Exac | rs77672568 |
Gnomad | rs77672568 |
Varsome | rs77672568 |
LitVar | rs77672568 |
Map | rs77672568 |
PheGenI | rs77672568 |
Biobank | rs77672568 |
1000 genomes | rs77672568 |
hgdp | rs77672568 |
ensembl | rs77672568 |
geneview | rs77672568 |
scholar | rs77672568 |
rs77672568 | |
pharmgkb | rs77672568 |
gwascentral | rs77672568 |
openSNP | rs77672568 |
23andMe | rs77672568 |
SNPshot | rs77672568 |
SNPdbe | rs77672568 |
MSV3d | rs77672568 |
GWAS Ctlg | rs77672568 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77672568(G;G) |
Alt | rs77672568(G;G) |
Reference | Rs77672568(-;-) |
Significance | Pathogenic |
Disease | Aicardi Goutieres syndrome 4 |
Variation | info |
Gene | RNASEH2A |
CLNDBN | Aicardi Goutieres syndrome 4 |
Reversed | 0 |
HGVS | NC_000019.9:g.12918027dupG |
CLNSRC | ClinVar |
CLNACC | RCV000114337.2, |