rs121909639
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121909639(C;T) |
Make rs121909639(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 38415899 |
Gene | FGFR1 |
is a | snp |
is | mentioned by |
dbSNP | rs121909639 |
dbSNP (classic) | rs121909639 |
ClinGen | rs121909639 |
ebi | rs121909639 |
HLI | rs121909639 |
Exac | rs121909639 |
Gnomad | rs121909639 |
Varsome | rs121909639 |
LitVar | rs121909639 |
Map | rs121909639 |
PheGenI | rs121909639 |
Biobank | rs121909639 |
1000 genomes | rs121909639 |
hgdp | rs121909639 |
ensembl | rs121909639 |
geneview | rs121909639 |
scholar | rs121909639 |
rs121909639 | |
pharmgkb | rs121909639 |
gwascentral | rs121909639 |
openSNP | rs121909639 |
23andMe | rs121909639 |
SNPshot | rs121909639 |
SNPdbe | rs121909639 |
MSV3d | rs121909639 |
GWAS Ctlg | rs121909639 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909639(T;T) |
Alt | rs121909639(T;T) |
Reference | Rs121909639(C;C) |
Significance | Other |
Disease | HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA not provided |
Variation | info |
Gene | FGFR1 |
CLNDBN | HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA, SUSCEPTIBILITY TO not provided |
Reversed | 1 |
HGVS | NC_000008.10:g.38273417G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000030934.2, RCV000478244.1, |