rs104893635
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs104893635(A;G) |
Make rs104893635(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 176094672 |
Gene | HOXD13 |
is a | snp |
is | mentioned by |
dbSNP | rs104893635 |
dbSNP (old) | rs104893635 |
ClinGen | rs104893635 |
ebi | rs104893635 |
HLI | rs104893635 |
Exac | rs104893635 |
Gnomad | rs104893635 |
Varsome | rs104893635 |
Map | rs104893635 |
PheGenI | rs104893635 |
Biobank | rs104893635 |
1000 genomes | rs104893635 |
hgdp | rs104893635 |
ensembl | rs104893635 |
gopubmed | rs104893635 |
geneview | rs104893635 |
scholar | rs104893635 |
rs104893635 | |
pharmgkb | rs104893635 |
gwascentral | rs104893635 |
openSNP | rs104893635 |
23andMe | rs104893635 |
23andMe all | rs104893635 |
SNPshot | rs104893635 |
SNPdbe | rs104893635 |
MSV3d | rs104893635 |
GWAS Ctlg | rs104893635 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104893635(G;G) |
Alt | rs104893635(G;G) |
Reference | Rs104893635(A;A) |
Significance | Pathogenic |
Disease | Syndactyly |
Variation | info |
Gene | HOXD13 |
CLNDBN | Syndactyly, type V |
Reversed | 0 |
HGVS | NC_000002.11:g.176959400A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000016002.26, |