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

rs1085307771

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome17
Position17215284
GeneFLCN
is asnp
is mentioned by
dbSNPrs1085307771
dbSNP (classic)rs1085307771
ClinGenrs1085307771
ebirs1085307771
HLIrs1085307771
Exacrs1085307771
Gnomadrs1085307771
Varsomers1085307771
LitVarrs1085307771
Maprs1085307771
PheGenIrs1085307771
Biobankrs1085307771
1000 genomesrs1085307771
hgdprs1085307771
ensemblrs1085307771
geneviewrs1085307771
scholarrs1085307771
googlers1085307771
pharmgkbrs1085307771
gwascentralrs1085307771
openSNPrs1085307771
23andMers1085307771
23andMe allrs1085307771
SNPshotrs1085307771
SNPdbers1085307771
MSV3drs1085307771
GWAS Ctlgrs1085307771
Max Magnitude0
ClinVar
Risk rs1085307771(AGCC;AGCC)
Alt rs1085307771(AGCC;AGCC)
Reference Rs1085307771(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17118599_17118602dup
CLNSRC
CLNACC RCV000489234.1,