rs606231408
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs606231408(C;G) |
Make rs606231408(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 101774832 |
Gene | FGF8 |
is a | snp |
is | mentioned by |
dbSNP | rs606231408 |
dbSNP (classic) | rs606231408 |
ClinGen | rs606231408 |
ebi | rs606231408 |
HLI | rs606231408 |
Exac | rs606231408 |
Gnomad | rs606231408 |
Varsome | rs606231408 |
LitVar | rs606231408 |
Map | rs606231408 |
PheGenI | rs606231408 |
Biobank | rs606231408 |
1000 genomes | rs606231408 |
hgdp | rs606231408 |
ensembl | rs606231408 |
geneview | rs606231408 |
scholar | rs606231408 |
rs606231408 | |
pharmgkb | rs606231408 |
gwascentral | rs606231408 |
openSNP | rs606231408 |
23andMe | rs606231408 |
SNPshot | rs606231408 |
SNPdbe | rs606231408 |
MSV3d | rs606231408 |
GWAS Ctlg | rs606231408 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs606231408(G;G) |
Alt | rs606231408(G;G) |
Reference | Rs606231408(C;C) |
Significance | Probable-Pathogenic |
Disease | Kallmann syndrome 6 |
Variation | info |
Gene | FGF8 |
CLNDBN | Kallmann syndrome 6 |
Reversed | 1 |
HGVS | NC_000010.10:g.103534589G>C |
CLNSRC | |
CLNACC | RCV000128829.1, |