rs104893839
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs104893839(A;A) |
Make rs104893839(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 67744659 |
Gene | GNRHR |
is a | snp |
is | mentioned by |
dbSNP | rs104893839 |
dbSNP (classic) | rs104893839 |
ClinGen | rs104893839 |
ebi | rs104893839 |
HLI | rs104893839 |
Exac | rs104893839 |
Gnomad | rs104893839 |
Varsome | rs104893839 |
LitVar | rs104893839 |
Map | rs104893839 |
PheGenI | rs104893839 |
Biobank | rs104893839 |
1000 genomes | rs104893839 |
hgdp | rs104893839 |
ensembl | rs104893839 |
geneview | rs104893839 |
scholar | rs104893839 |
rs104893839 | |
pharmgkb | rs104893839 |
gwascentral | rs104893839 |
openSNP | rs104893839 |
23andMe | rs104893839 |
SNPshot | rs104893839 |
SNPdbe | rs104893839 |
MSV3d | rs104893839 |
GWAS Ctlg | rs104893839 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104893839(A;A) |
Alt | rs104893839(A;A) |
Reference | Rs104893839(C;C) |
Significance | Pathogenic |
Disease | Hypogonadotropic hypogonadism 7 with or without anosmia |
Variation | info |
Gene | GNRHR |
CLNDBN | Hypogonadotropic hypogonadism 7 with or without anosmia |
Reversed | 1 |
HGVS | NC_000004.11:g.68610377G>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000030911.29, |