rs121917779
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs121917779(A;C) |
Make rs121917779(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 41201565 |
Gene | C6 |
is a | snp |
is | mentioned by |
dbSNP | rs121917779 |
dbSNP (classic) | rs121917779 |
ClinGen | rs121917779 |
ebi | rs121917779 |
HLI | rs121917779 |
Exac | rs121917779 |
Gnomad | rs121917779 |
Varsome | rs121917779 |
LitVar | rs121917779 |
Map | rs121917779 |
PheGenI | rs121917779 |
Biobank | rs121917779 |
1000 genomes | rs121917779 |
hgdp | rs121917779 |
ensembl | rs121917779 |
geneview | rs121917779 |
scholar | rs121917779 |
rs121917779 | |
pharmgkb | rs121917779 |
gwascentral | rs121917779 |
openSNP | rs121917779 |
23andMe | rs121917779 |
SNPshot | rs121917779 |
SNPdbe | rs121917779 |
MSV3d | rs121917779 |
GWAS Ctlg | rs121917779 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121917779(C;C) rs121917779(G;G) |
Alt | rs121917779(C;C) rs121917779(G;G) |
Reference | Rs121917779(A;A) |
Significance | Non-pathogenic |
Disease | C6 A/B POLYMORPHISM |
Variation | info |
Gene | C6 |
CLNDBN | C6 A/B POLYMORPHISM |
Reversed | 1 |
HGVS | NC_000005.9:g.41201667T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000012896.2, |