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rs1064793128

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Chromosome17
Position17215237
GeneFLCN
is asnp
is mentioned by
dbSNPrs1064793128
dbSNP (old)rs1064793128
ClinGenrs1064793128
ebirs1064793128
HLIrs1064793128
Exacrs1064793128
Gnomadrs1064793128
Varsomers1064793128
Maprs1064793128
PheGenIrs1064793128
Biobankrs1064793128
1000 genomesrs1064793128
hgdprs1064793128
ensemblrs1064793128
gopubmedrs1064793128
geneviewrs1064793128
scholarrs1064793128
googlers1064793128
pharmgkbrs1064793128
gwascentralrs1064793128
openSNPrs1064793128
23andMers1064793128
23andMe allrs1064793128
SNPshotrs1064793128
SNPdbers1064793128
MSV3drs1064793128
GWAS Ctlgrs1064793128
Max Magnitude0
ClinVar
Risk rs1064793128(-;-)
Alt rs1064793128(-;-)
Reference Rs1064793128(TC;TC)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene FLCN
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.17118551_17118552delGA
CLNSRC
CLNACC RCV000485073.1, RCV000492502.1,