rs886039769
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs886039769(C;T) |
Make rs886039769(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 124500686 |
Gene | NR5A1 |
is a | snp |
is | mentioned by |
dbSNP | rs886039769 |
dbSNP (classic) | rs886039769 |
ClinGen | rs886039769 |
ebi | rs886039769 |
HLI | rs886039769 |
Exac | rs886039769 |
Gnomad | rs886039769 |
Varsome | rs886039769 |
LitVar | rs886039769 |
Map | rs886039769 |
PheGenI | rs886039769 |
Biobank | rs886039769 |
1000 genomes | rs886039769 |
hgdp | rs886039769 |
ensembl | rs886039769 |
geneview | rs886039769 |
scholar | rs886039769 |
rs886039769 | |
pharmgkb | rs886039769 |
gwascentral | rs886039769 |
openSNP | rs886039769 |
23andMe | rs886039769 |
SNPshot | rs886039769 |
SNPdbe | rs886039769 |
MSV3d | rs886039769 |
GWAS Ctlg | rs886039769 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886039769(T;T) |
Alt | rs886039769(T;T) |
Reference | Rs886039769(C;C) |
Significance | Other |
Disease | 46 |
Variation | info |
Gene | NR5A1 |
CLNDBN | 46,XY sex reversal, type 3 46,XX sex reversal 4 |
Reversed | 1 |
HGVS | NC_000009.11:g.127262965G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000256210.1, RCV000490553.1, |