rs41419545
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs41419545(C;T) |
Make rs41419545(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 17215284 |
Gene | FLCN |
is a | snp |
is | mentioned by |
dbSNP | rs41419545 |
dbSNP (classic) | rs41419545 |
ClinGen | rs41419545 |
ebi | rs41419545 |
HLI | rs41419545 |
Exac | rs41419545 |
Gnomad | rs41419545 |
Varsome | rs41419545 |
LitVar | rs41419545 |
Map | rs41419545 |
PheGenI | rs41419545 |
Biobank | rs41419545 |
1000 genomes | rs41419545 |
hgdp | rs41419545 |
ensembl | rs41419545 |
geneview | rs41419545 |
scholar | rs41419545 |
rs41419545 | |
pharmgkb | rs41419545 |
gwascentral | rs41419545 |
openSNP | rs41419545 |
23andMe | rs41419545 |
SNPshot | rs41419545 |
SNPdbe | rs41419545 |
MSV3d | rs41419545 |
GWAS Ctlg | rs41419545 |
GMAF | 0.001377 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41419545(A;A) rs41419545(T;T) |
Alt | rs41419545(A;A) rs41419545(T;T) |
Reference | Rs41419545(C;C) |
Significance | Other |
Disease | Carcinoma of colon not provided not specified Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas Spontaneous pneumothorax |
Variation | info |
Gene | FLCN LOC101928660 |
CLNDBN | Carcinoma of colon not provided not specified Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas Spontaneous pneumothorax |
Reversed | 0 |
HGVS | NC_000017.10:g.17118598C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000003537.5, RCV000034789.1, RCV000121112.4, RCV000163302.3, RCV000232087.4, RCV000336471.1, |
[PMID 19116017] Folliculin mutations are not associated with severe COPD.