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rs41419545

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41419545(C;T)
Make rs41419545(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position17215284
GeneFLCN, LOC101928660
is asnp
is mentioned by
dbSNPrs41419545
ebirs41419545
HLIrs41419545
Exacrs41419545
Varsomers41419545
Maprs41419545
PheGenIrs41419545
hapmaprs41419545
1000 genomesrs41419545
hgdprs41419545
ensemblrs41419545
gopubmedrs41419545
geneviewrs41419545
scholarrs41419545
googlers41419545
pharmgkbrs41419545
gwascentralrs41419545
openSNPrs41419545
23andMers41419545
23andMe allrs41419545
SNP Nexus

SNPshotrs41419545
SNPdbers41419545
MSV3drs41419545
GWAS Ctlgrs41419545
GMAF0.001377
Max Magnitude0
OMIM607273
Desc
Variant0008
Relatedalso


ClinVar
Risk rs41419545(T;T)
Alt rs41419545(T;T)
Reference rs41419545(C;C)
Significance Other
Disease Carcinoma of colon not provided not specified Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas
Variation info
Gene FLCN LOC101928660
CLNDBN Carcinoma of colon not provided not specified Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas
Reversed 0
HGVS NC_000017.10:g.17118598C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003537.4, RCV000034789.1, RCV000121112.2, RCV000163302.1, RCV000232087.2,



[PMID 19116017OA-icon.png] Folliculin mutations are not associated with severe COPD.