rs761543313
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs761543313(A;A) |
Make rs761543313(A;T) |
Make rs761543313(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 14 |
Position | 67600203 |
Gene | GPHN, LOC105370543, PIGH |
is a | snp |
is | mentioned by |
dbSNP | rs761543313 |
dbSNP (classic) | rs761543313 |
ClinGen | rs761543313 |
ebi | rs761543313 |
HLI | rs761543313 |
Exac | rs761543313 |
Gnomad | rs761543313 |
Varsome | rs761543313 |
LitVar | rs761543313 |
Map | rs761543313 |
PheGenI | rs761543313 |
Biobank | rs761543313 |
1000 genomes | rs761543313 |
hgdp | rs761543313 |
ensembl | rs761543313 |
geneview | rs761543313 |
scholar | rs761543313 |
rs761543313 | |
pharmgkb | rs761543313 |
gwascentral | rs761543313 |
openSNP | rs761543313 |
23andMe | rs761543313 |
SNPshot | rs761543313 |
SNPdbe | rs761543313 |
MSV3d | rs761543313 |
GWAS Ctlg | rs761543313 |
Max Magnitude | 0 |
aka NM_004569.4(PIGH):c.1A>T or (p.Met1Leu)
OMIM pathogenic variant