Have questions? Visit https://www.reddit.com/r/SNPedia

rs727504645

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504645(-;-)
Make rs727504645(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position17224094
GeneFLCN
is asnp
is mentioned by
dbSNPrs727504645
ebirs727504645
HLIrs727504645
Exacrs727504645
Varsomers727504645
Maprs727504645
PheGenIrs727504645
hapmaprs727504645
1000 genomesrs727504645
hgdprs727504645
ensemblrs727504645
gopubmedrs727504645
geneviewrs727504645
scholarrs727504645
googlers727504645
pharmgkbrs727504645
gwascentralrs727504645
openSNPrs727504645
23andMers727504645
23andMe allrs727504645
SNP Nexus

SNPshotrs727504645
SNPdbers727504645
MSV3drs727504645
GWAS Ctlgrs727504645
Max Magnitude0
ClinVar
Risk rs727504645(;)
Alt rs727504645(;)
Reference rs727504645(G;G)
Significance Probable-Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17127408delC
CLNSRC
CLNACC RCV000155908.1,