rs757966746
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs757966746(A;A) |
Make rs757966746(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 34294083 |
Gene | AHCY |
is a | snp |
is | mentioned by |
dbSNP | rs757966746 |
dbSNP (classic) | rs757966746 |
ClinGen | rs757966746 |
ebi | rs757966746 |
HLI | rs757966746 |
Exac | rs757966746 |
Gnomad | rs757966746 |
Varsome | rs757966746 |
LitVar | rs757966746 |
Map | rs757966746 |
PheGenI | rs757966746 |
Biobank | rs757966746 |
1000 genomes | rs757966746 |
hgdp | rs757966746 |
ensembl | rs757966746 |
geneview | rs757966746 |
scholar | rs757966746 |
rs757966746 | |
pharmgkb | rs757966746 |
gwascentral | rs757966746 |
openSNP | rs757966746 |
23andMe | rs757966746 |
SNPshot | rs757966746 |
SNPdbe | rs757966746 |
MSV3d | rs757966746 |
GWAS Ctlg | rs757966746 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757966746(A;A) |
Alt | rs757966746(A;A) |
Reference | Rs757966746(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | AHCY |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.32881889G>A |
CLNSRC | |
CLNACC | RCV000223995.1, |