rs773457070
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs773457070(G;T) |
Make rs773457070(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 6955368 |
Gene | LAMA1, LOC101927188 |
is a | snp |
is | mentioned by |
dbSNP | rs773457070 |
dbSNP (classic) | rs773457070 |
ClinGen | rs773457070 |
ebi | rs773457070 |
HLI | rs773457070 |
Exac | rs773457070 |
Gnomad | rs773457070 |
Varsome | rs773457070 |
LitVar | rs773457070 |
Map | rs773457070 |
PheGenI | rs773457070 |
Biobank | rs773457070 |
1000 genomes | rs773457070 |
hgdp | rs773457070 |
ensembl | rs773457070 |
geneview | rs773457070 |
scholar | rs773457070 |
rs773457070 | |
pharmgkb | rs773457070 |
gwascentral | rs773457070 |
openSNP | rs773457070 |
23andMe | rs773457070 |
SNPshot | rs773457070 |
SNPdbe | rs773457070 |
MSV3d | rs773457070 |
GWAS Ctlg | rs773457070 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773457070(T;T) |
Alt | rs773457070(T;T) |
Reference | Rs773457070(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LOC101927188 LAMA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.6955367G>T |
CLNSRC | |
CLNACC | RCV000413473.1, |