Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060502370

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502370(-;-)
Make rs1060502370(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17227936
GeneFLCN
is asnp
is mentioned by
dbSNPrs1060502370
dbSNP (old)rs1060502370
ClinGenrs1060502370
ebirs1060502370
HLIrs1060502370
Exacrs1060502370
Gnomadrs1060502370
Varsomers1060502370
Maprs1060502370
PheGenIrs1060502370
Biobankrs1060502370
1000 genomesrs1060502370
hgdprs1060502370
ensemblrs1060502370
gopubmedrs1060502370
geneviewrs1060502370
scholarrs1060502370
googlers1060502370
pharmgkbrs1060502370
gwascentralrs1060502370
openSNPrs1060502370
23andMers1060502370
23andMe allrs1060502370
SNPshotrs1060502370
SNPdbers1060502370
MSV3drs1060502370
GWAS Ctlgrs1060502370
Max Magnitude0
ClinVar
Risk rs1060502370(-;-)
Alt rs1060502370(-;-)
Reference Rs1060502370(A;A)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17131250delT
CLNSRC
CLNACC RCV000468103.1,