rs727503442
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GTGGA;GTGGA) | 0 | common in clinvar |
Make rs727503442(-;-) |
Make rs727503442(-;GTGGA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 43600916 |
Gene | STRC |
is a | snp |
is | mentioned by |
dbSNP | rs727503442 |
dbSNP (classic) | rs727503442 |
ClinGen | rs727503442 |
ebi | rs727503442 |
HLI | rs727503442 |
Exac | rs727503442 |
Gnomad | rs727503442 |
Varsome | rs727503442 |
LitVar | rs727503442 |
Map | rs727503442 |
PheGenI | rs727503442 |
Biobank | rs727503442 |
1000 genomes | rs727503442 |
hgdp | rs727503442 |
ensembl | rs727503442 |
geneview | rs727503442 |
scholar | rs727503442 |
rs727503442 | |
pharmgkb | rs727503442 |
gwascentral | rs727503442 |
openSNP | rs727503442 |
23andMe | rs727503442 |
SNPshot | rs727503442 |
SNPdbe | rs727503442 |
MSV3d | rs727503442 |
GWAS Ctlg | rs727503442 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727503442(-;-) |
Alt | rs727503442(-;-) |
Reference | Rs727503442(GTGGA;GTGGA) |
Significance | Pathogenic |
Disease | Nonsyndromic hearing loss and deafness |
Variation | info |
Gene | STRC |
CLNDBN | Nonsyndromic hearing loss and deafness |
Reversed | 1 |
HGVS | NC_000015.9:g.43893114_43893118delTCCAC |
CLNSRC | |
CLNACC | RCV000151941.1, |