rs863223984
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs863223984(-;AATGACAAGAATAAAAGCTGC) |
Make rs863223984(AATGACAAGAATAAAAGCTGC;AATGACAAGAATAAAAGCTGC) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 241506112 |
Gene | FH |
is a | snp |
is | mentioned by |
dbSNP | rs863223984 |
dbSNP (classic) | rs863223984 |
ClinGen | rs863223984 |
ebi | rs863223984 |
HLI | rs863223984 |
Exac | rs863223984 |
Gnomad | rs863223984 |
Varsome | rs863223984 |
LitVar | rs863223984 |
Map | rs863223984 |
PheGenI | rs863223984 |
Biobank | rs863223984 |
1000 genomes | rs863223984 |
hgdp | rs863223984 |
ensembl | rs863223984 |
geneview | rs863223984 |
scholar | rs863223984 |
rs863223984 | |
pharmgkb | rs863223984 |
gwascentral | rs863223984 |
openSNP | rs863223984 |
23andMe | rs863223984 |
SNPshot | rs863223984 |
SNPdbe | rs863223984 |
MSV3d | rs863223984 |
GWAS Ctlg | rs863223984 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223984(AATGACAAGAATAAAAGCTGC;AATGACAAGAATAAAAGCTGC) |
Alt | rs863223984(AATGACAAGAATAAAAGCTGC;AATGACAAGAATAAAAGCTGC) |
Reference | Rs863223984(-;-) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FH |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000001.10:g.241669413_241669433dup21 |
CLNSRC | |
CLNACC | RCV000199721.1, |