rs41341748
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs41341748(A;A) |
Make rs41341748(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 16155085 |
Gene | MSR1 |
is a | snp |
is | mentioned by |
dbSNP | rs41341748 |
dbSNP (classic) | rs41341748 |
ClinGen | rs41341748 |
ebi | rs41341748 |
HLI | rs41341748 |
Exac | rs41341748 |
Gnomad | rs41341748 |
Varsome | rs41341748 |
LitVar | rs41341748 |
Map | rs41341748 |
PheGenI | rs41341748 |
Biobank | rs41341748 |
1000 genomes | rs41341748 |
hgdp | rs41341748 |
ensembl | rs41341748 |
geneview | rs41341748 |
scholar | rs41341748 |
rs41341748 | |
pharmgkb | rs41341748 |
gwascentral | rs41341748 |
openSNP | rs41341748 |
23andMe | rs41341748 |
SNPshot | rs41341748 |
SNPdbe | rs41341748 |
MSV3d | rs41341748 |
GWAS Ctlg | rs41341748 |
GMAF | 0.007805 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41341748(A;A) rs41341748(C;C) |
Alt | rs41341748(A;A) rs41341748(C;C) |
Reference | Rs41341748(G;G) |
Significance | Pathogenic |
Disease | Malignant tumor of prostate Hereditary cancer-predisposing syndrome not specified |
Variation | info |
Gene | MSR1 |
CLNDBN | Malignant tumor of prostate Hereditary cancer-predisposing syndrome not specified |
Reversed | 0 |
HGVS | NC_000008.10:g.16012594G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000015431.21, RCV000210798.1, RCV000481066.1, |