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rs1085307478

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCATCAT;CCATCAT) 0 common in clinvar
Chromosome17
Position17224013
GeneFLCN
is asnp
is mentioned by
dbSNPrs1085307478
dbSNP (old)rs1085307478
ClinGenrs1085307478
ebirs1085307478
HLIrs1085307478
Exacrs1085307478
Gnomadrs1085307478
Varsomers1085307478
LitVarrs1085307478
Maprs1085307478
PheGenIrs1085307478
Biobankrs1085307478
1000 genomesrs1085307478
hgdprs1085307478
ensemblrs1085307478
gopubmedrs1085307478
geneviewrs1085307478
scholarrs1085307478
googlers1085307478
pharmgkbrs1085307478
gwascentralrs1085307478
openSNPrs1085307478
23andMers1085307478
23andMe allrs1085307478
SNPshotrs1085307478
SNPdbers1085307478
MSV3drs1085307478
GWAS Ctlgrs1085307478
Max Magnitude0
ClinVar
Risk rs1085307478(-;-)
Alt rs1085307478(-;-)
Reference Rs1085307478(CCATCAT;CCATCAT)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17127327_17127333delATGATGG
CLNSRC
CLNACC RCV000489049.1,