rs116207524
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs116207524(A;A) |
Make rs116207524(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 148483196 |
Gene | MBD5 |
is a | snp |
is | mentioned by |
dbSNP | rs116207524 |
dbSNP (classic) | rs116207524 |
ClinGen | rs116207524 |
ebi | rs116207524 |
HLI | rs116207524 |
Exac | rs116207524 |
Gnomad | rs116207524 |
Varsome | rs116207524 |
LitVar | rs116207524 |
Map | rs116207524 |
PheGenI | rs116207524 |
Biobank | rs116207524 |
1000 genomes | rs116207524 |
hgdp | rs116207524 |
ensembl | rs116207524 |
geneview | rs116207524 |
scholar | rs116207524 |
rs116207524 | |
pharmgkb | rs116207524 |
gwascentral | rs116207524 |
openSNP | rs116207524 |
23andMe | rs116207524 |
SNPshot | rs116207524 |
SNPdbe | rs116207524 |
MSV3d | rs116207524 |
GWAS Ctlg | rs116207524 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs116207524(A;A) rs116207524(T;T) |
Alt | rs116207524(A;A) rs116207524(T;T) |
Reference | Rs116207524(G;G) |
Significance | Other |
Disease | not specified Intellectual Disability |
Variation | info |
Gene | MBD5 |
CLNDBN | not specified Intellectual Disability, Dominant |
Reversed | 0 |
HGVS | NC_000002.11:g.149240765G>A |
CLNSRC | |
CLNACC | RCV000081949.6, RCV000288037.1, |