rs72658163
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs72658163(A;A) |
Make rs72658163(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 94420276 |
Gene | COL1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs72658163 |
dbSNP (classic) | rs72658163 |
ClinGen | rs72658163 |
ebi | rs72658163 |
HLI | rs72658163 |
Exac | rs72658163 |
Gnomad | rs72658163 |
Varsome | rs72658163 |
LitVar | rs72658163 |
Map | rs72658163 |
PheGenI | rs72658163 |
Biobank | rs72658163 |
1000 genomes | rs72658163 |
hgdp | rs72658163 |
ensembl | rs72658163 |
geneview | rs72658163 |
scholar | rs72658163 |
rs72658163 | |
pharmgkb | rs72658163 |
gwascentral | rs72658163 |
openSNP | rs72658163 |
23andMe | rs72658163 |
SNPshot | rs72658163 |
SNPdbe | rs72658163 |
MSV3d | rs72658163 |
GWAS Ctlg | rs72658163 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72658163(A;A) |
Alt | rs72658163(A;A) |
Reference | Rs72658163(G;G) |
Significance | Unknown |
Disease | Marfan syndrome not specified |
Variation | info |
Gene | COL1A2 |
CLNDBN | Marfan syndrome, atypical not specified |
Reversed | 0 |
HGVS | NC_000007.13:g.94049588G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000018790.4, RCV000413739.1, |