rs121964944
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs121964944(A;G) |
Make rs121964944(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 113129542 |
Gene | F10, F10-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs121964944 |
dbSNP (classic) | rs121964944 |
ClinGen | rs121964944 |
ebi | rs121964944 |
HLI | rs121964944 |
Exac | rs121964944 |
Gnomad | rs121964944 |
Varsome | rs121964944 |
LitVar | rs121964944 |
Map | rs121964944 |
PheGenI | rs121964944 |
Biobank | rs121964944 |
1000 genomes | rs121964944 |
hgdp | rs121964944 |
ensembl | rs121964944 |
geneview | rs121964944 |
scholar | rs121964944 |
rs121964944 | |
pharmgkb | rs121964944 |
gwascentral | rs121964944 |
openSNP | rs121964944 |
23andMe | rs121964944 |
SNPshot | rs121964944 |
SNPdbe | rs121964944 |
MSV3d | rs121964944 |
GWAS Ctlg | rs121964944 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121964944(G;G) |
Alt | rs121964944(G;G) |
Reference | Rs121964944(A;A) |
Significance | Untested |
Disease | |
Variation | info |
Gene | F10 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000013.10:g.113783856A>G |
CLNSRC | |
CLNACC |