rs876661331
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs876661331(A;A) |
Make rs876661331(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 101770447 |
Gene | FGF8, LOC105378457 |
is a | snp |
is | mentioned by |
dbSNP | rs876661331 |
dbSNP (classic) | rs876661331 |
ClinGen | rs876661331 |
ebi | rs876661331 |
HLI | rs876661331 |
Exac | rs876661331 |
Gnomad | rs876661331 |
Varsome | rs876661331 |
LitVar | rs876661331 |
Map | rs876661331 |
PheGenI | rs876661331 |
Biobank | rs876661331 |
1000 genomes | rs876661331 |
hgdp | rs876661331 |
ensembl | rs876661331 |
geneview | rs876661331 |
scholar | rs876661331 |
rs876661331 | |
pharmgkb | rs876661331 |
gwascentral | rs876661331 |
openSNP | rs876661331 |
23andMe | rs876661331 |
SNPshot | rs876661331 |
SNPdbe | rs876661331 |
MSV3d | rs876661331 |
GWAS Ctlg | rs876661331 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661331(A;A) |
Alt | rs876661331(A;A) |
Reference | Rs876661331(G;G) |
Significance | Probable-Pathogenic |
Disease | Holoprosencephaly |
Variation | info |
Gene | FGF8 |
CLNDBN | Holoprosencephaly |
Reversed | 1 |
HGVS | NC_000010.10:g.103530204C>T |
CLNSRC | |
CLNACC | RCV000223812.1, |