rs776038451
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs776038451(A;A) |
Make rs776038451(A;G) |
Make rs776038451(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 14 |
Position | 67593826 |
Gene | GPHN, PIGH |
is a | snp |
is | mentioned by |
dbSNP | rs776038451 |
dbSNP (classic) | rs776038451 |
ClinGen | rs776038451 |
ebi | rs776038451 |
HLI | rs776038451 |
Exac | rs776038451 |
Gnomad | rs776038451 |
Varsome | rs776038451 |
LitVar | rs776038451 |
Map | rs776038451 |
PheGenI | rs776038451 |
Biobank | rs776038451 |
1000 genomes | rs776038451 |
hgdp | rs776038451 |
ensembl | rs776038451 |
geneview | rs776038451 |
scholar | rs776038451 |
rs776038451 | |
pharmgkb | rs776038451 |
gwascentral | rs776038451 |
openSNP | rs776038451 |
23andMe | rs776038451 |
SNPshot | rs776038451 |
SNPdbe | rs776038451 |
MSV3d | rs776038451 |
GWAS Ctlg | rs776038451 |
Max Magnitude | 0 |
aka NM_004569.4(PIGH):c.307T>C or (p.Ser103Pro)
OMIM pathogenic variant