rs876661179
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GAC;GAC) | 0 | common in clinvar |
Make rs876661179(-;-) |
Make rs876661179(-;GAC) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 14 |
Position | 23415188 |
Gene | MHRT, MYH7 |
is a | snp |
is | mentioned by |
dbSNP | rs876661179 |
dbSNP (classic) | rs876661179 |
ClinGen | rs876661179 |
ebi | rs876661179 |
HLI | rs876661179 |
Exac | rs876661179 |
Gnomad | rs876661179 |
Varsome | rs876661179 |
LitVar | rs876661179 |
Map | rs876661179 |
PheGenI | rs876661179 |
Biobank | rs876661179 |
1000 genomes | rs876661179 |
hgdp | rs876661179 |
ensembl | rs876661179 |
geneview | rs876661179 |
scholar | rs876661179 |
rs876661179 | |
pharmgkb | rs876661179 |
gwascentral | rs876661179 |
openSNP | rs876661179 |
23andMe | rs876661179 |
SNPshot | rs876661179 |
SNPdbe | rs876661179 |
MSV3d | rs876661179 |
GWAS Ctlg | rs876661179 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661179(-;-) |
Alt | rs876661179(-;-) |
Reference | Rs876661179(GAC;GAC) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MYH7 MHRT |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000014.8:g.23884397_23884399delGTC |
CLNSRC | |
CLNACC | RCV000219460.1, |