rs763399323
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs763399323(C;T) |
Make rs763399323(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 84200638 |
Gene | CDHR1 |
is a | snp |
is | mentioned by |
dbSNP | rs763399323 |
dbSNP (classic) | rs763399323 |
ClinGen | rs763399323 |
ebi | rs763399323 |
HLI | rs763399323 |
Exac | rs763399323 |
Gnomad | rs763399323 |
Varsome | rs763399323 |
LitVar | rs763399323 |
Map | rs763399323 |
PheGenI | rs763399323 |
Biobank | rs763399323 |
1000 genomes | rs763399323 |
hgdp | rs763399323 |
ensembl | rs763399323 |
geneview | rs763399323 |
scholar | rs763399323 |
rs763399323 | |
pharmgkb | rs763399323 |
gwascentral | rs763399323 |
openSNP | rs763399323 |
23andMe | rs763399323 |
SNPshot | rs763399323 |
SNPdbe | rs763399323 |
MSV3d | rs763399323 |
GWAS Ctlg | rs763399323 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763399323(A;A) rs763399323(T;T) |
Alt | rs763399323(A;A) rs763399323(T;T) |
Reference | Rs763399323(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CDHR1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.85960394C>A |
CLNSRC | |
CLNACC | RCV000171179.1, |