rs77543610
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs77543610(C;C) |
Make rs77543610(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 121520160 |
Gene | FGFR2 |
is a | snp |
is | mentioned by |
dbSNP | rs77543610 |
dbSNP (classic) | rs77543610 |
ClinGen | rs77543610 |
ebi | rs77543610 |
HLI | rs77543610 |
Exac | rs77543610 |
Gnomad | rs77543610 |
Varsome | rs77543610 |
LitVar | rs77543610 |
Map | rs77543610 |
PheGenI | rs77543610 |
Biobank | rs77543610 |
1000 genomes | rs77543610 |
hgdp | rs77543610 |
ensembl | rs77543610 |
geneview | rs77543610 |
scholar | rs77543610 |
rs77543610 | |
pharmgkb | rs77543610 |
gwascentral | rs77543610 |
openSNP | rs77543610 |
23andMe | rs77543610 |
SNPshot | rs77543610 |
SNPdbe | rs77543610 |
MSV3d | rs77543610 |
GWAS Ctlg | rs77543610 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77543610(C;C) |
Alt | rs77543610(C;C) |
Reference | Rs77543610(G;G) |
Significance | Pathogenic |
Disease | Acrocephalosyndactyly type I Head and Neck Neoplasms not provided |
Variation | info |
Gene | FGFR2 |
CLNDBN | Acrocephalosyndactyly type I Head and Neck Neoplasms not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.123279674G>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000014193.24, RCV000436870.1, RCV000489611.1, |