rs386833512
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs386833512(A;A) |
Make rs386833512(A;C) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 2 |
Position | 48963061 |
Gene | FSHR |
is a | snp |
is | mentioned by |
dbSNP | rs386833512 |
dbSNP (classic) | rs386833512 |
ClinGen | rs386833512 |
ebi | rs386833512 |
HLI | rs386833512 |
Exac | rs386833512 |
Gnomad | rs386833512 |
Varsome | rs386833512 |
LitVar | rs386833512 |
Map | rs386833512 |
PheGenI | rs386833512 |
Biobank | rs386833512 |
1000 genomes | rs386833512 |
hgdp | rs386833512 |
ensembl | rs386833512 |
geneview | rs386833512 |
scholar | rs386833512 |
rs386833512 | |
pharmgkb | rs386833512 |
gwascentral | rs386833512 |
openSNP | rs386833512 |
23andMe | rs386833512 |
SNPshot | rs386833512 |
SNPdbe | rs386833512 |
MSV3d | rs386833512 |
GWAS Ctlg | rs386833512 |
Max Magnitude | 0 |
aka NM_000145.3(FSHR):c.1760C>A or (p.Pro587His)
OMIM pathogenic variant