rs104894701
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs104894701(C;T) |
Make rs104894701(T;T) |
Reference | GRCh37 37.1/132 |
Chromosome | 19 |
Position | 920542 |
Gene | KISS1R |
is a | snp |
is | mentioned by |
dbSNP | rs104894701 |
dbSNP (classic) | rs104894701 |
ClinGen | rs104894701 |
ebi | rs104894701 |
HLI | rs104894701 |
Exac | rs104894701 |
Gnomad | rs104894701 |
Varsome | rs104894701 |
LitVar | rs104894701 |
Map | rs104894701 |
PheGenI | rs104894701 |
Biobank | rs104894701 |
1000 genomes | rs104894701 |
hgdp | rs104894701 |
ensembl | rs104894701 |
geneview | rs104894701 |
scholar | rs104894701 |
rs104894701 | |
pharmgkb | rs104894701 |
gwascentral | rs104894701 |
openSNP | rs104894701 |
23andMe | rs104894701 |
SNPshot | rs104894701 |
SNPdbe | rs104894701 |
MSV3d | rs104894701 |
GWAS Ctlg | rs104894701 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104894701(T;T) |
Alt | rs104894701(T;T) |
Reference | Rs104894701(C;C) |
Significance | Pathogenic |
Disease | Hypogonadotropic hypogonadism 8 without anosmia |
Variation | info |
Gene | KISS1R |
CLNDBN | Hypogonadotropic hypogonadism 8 without anosmia |
Reversed | 0 |
HGVS | NC_000019.9:g.920542C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000030879.3, |