rs377461670
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs377461670(A;A) |
Make rs377461670(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 23415757 |
Gene | MHRT, MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs377461670 |
dbSNP (classic) | rs377461670 |
ClinGen | rs377461670 |
ebi | rs377461670 |
HLI | rs377461670 |
Exac | rs377461670 |
Gnomad | rs377461670 |
Varsome | rs377461670 |
LitVar | rs377461670 |
Map | rs377461670 |
PheGenI | rs377461670 |
Biobank | rs377461670 |
1000 genomes | rs377461670 |
hgdp | rs377461670 |
ensembl | rs377461670 |
geneview | rs377461670 |
scholar | rs377461670 |
rs377461670 | |
pharmgkb | rs377461670 |
gwascentral | rs377461670 |
openSNP | rs377461670 |
23andMe | rs377461670 |
SNPshot | rs377461670 |
SNPdbe | rs377461670 |
MSV3d | rs377461670 |
GWAS Ctlg | rs377461670 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs377461670(A;A) |
Alt | rs377461670(A;A) |
Reference | Rs377461670(G;G) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | MYH7 MHRT |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000014.8:g.23884966G>A |
CLNSRC | |
CLNACC | RCV000158681.2, |