rs757576534
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs757576534(A;A) |
Make rs757576534(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 35657873 |
Gene | CCDC107, RMRP |
is a | snp |
is | mentioned by |
dbSNP | rs757576534 |
dbSNP (classic) | rs757576534 |
ClinGen | rs757576534 |
ebi | rs757576534 |
HLI | rs757576534 |
Exac | rs757576534 |
Gnomad | rs757576534 |
Varsome | rs757576534 |
LitVar | rs757576534 |
Map | rs757576534 |
PheGenI | rs757576534 |
Biobank | rs757576534 |
1000 genomes | rs757576534 |
hgdp | rs757576534 |
ensembl | rs757576534 |
geneview | rs757576534 |
scholar | rs757576534 |
rs757576534 | |
pharmgkb | rs757576534 |
gwascentral | rs757576534 |
openSNP | rs757576534 |
23andMe | rs757576534 |
SNPshot | rs757576534 |
SNPdbe | rs757576534 |
MSV3d | rs757576534 |
GWAS Ctlg | rs757576534 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757576534(A;A) rs757576534(T;T) |
Alt | rs757576534(A;A) rs757576534(T;T) |
Reference | Rs757576534(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CCDC107 RMRP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.35657870G>A |
CLNSRC | |
CLNACC | RCV000423534.1, |