rs72658103
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs72658103(A;A) |
Make rs72658103(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 7 |
Position | 94410438 |
Gene | COL1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs72658103 |
dbSNP (classic) | rs72658103 |
ClinGen | rs72658103 |
ebi | rs72658103 |
HLI | rs72658103 |
Exac | rs72658103 |
Gnomad | rs72658103 |
Varsome | rs72658103 |
LitVar | rs72658103 |
Map | rs72658103 |
PheGenI | rs72658103 |
Biobank | rs72658103 |
1000 genomes | rs72658103 |
hgdp | rs72658103 |
ensembl | rs72658103 |
geneview | rs72658103 |
scholar | rs72658103 |
rs72658103 | |
pharmgkb | rs72658103 |
gwascentral | rs72658103 |
openSNP | rs72658103 |
23andMe | rs72658103 |
SNPshot | rs72658103 |
SNPdbe | rs72658103 |
MSV3d | rs72658103 |
GWAS Ctlg | rs72658103 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72658103(A;A) rs72658103(T;T) |
Alt | rs72658103(A;A) rs72658103(T;T) |
Reference | Rs72658103(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL1A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.94039750G>T |
CLNSRC | |
CLNACC | RCV000254840.1, |