rs59601651
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs59601651(C;T) |
Make rs59601651(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 156138537 |
Gene | LMNA |
is a | snp |
is | mentioned by |
dbSNP | rs59601651 |
dbSNP (classic) | rs59601651 |
ClinGen | rs59601651 |
ebi | rs59601651 |
HLI | rs59601651 |
Exac | rs59601651 |
Gnomad | rs59601651 |
Varsome | rs59601651 |
LitVar | rs59601651 |
Map | rs59601651 |
PheGenI | rs59601651 |
Biobank | rs59601651 |
1000 genomes | rs59601651 |
hgdp | rs59601651 |
ensembl | rs59601651 |
geneview | rs59601651 |
scholar | rs59601651 |
rs59601651 | |
pharmgkb | rs59601651 |
gwascentral | rs59601651 |
openSNP | rs59601651 |
23andMe | rs59601651 |
SNPshot | rs59601651 |
SNPdbe | rs59601651 |
MSV3d | rs59601651 |
GWAS Ctlg | rs59601651 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs59601651(G;G) rs59601651(T;T) |
Alt | rs59601651(G;G) rs59601651(T;T) |
Reference | Rs59601651(C;C) |
Significance | Untested |
Disease | not specified not provided |
Variation | info |
Gene | LMNA |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.156108328C>G; NC_000001.10:g.156108328C>T |
CLNSRC | |
CLNACC | RCV000155709.1, RCV000057354.3, RCV000235168.2, |