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rs1064793766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position17216378
GeneFLCN
is asnp
is mentioned by
dbSNPrs1064793766
dbSNP (old)rs1064793766
ClinGenrs1064793766
ebirs1064793766
HLIrs1064793766
Exacrs1064793766
Gnomadrs1064793766
Varsomers1064793766
Maprs1064793766
PheGenIrs1064793766
Biobankrs1064793766
1000 genomesrs1064793766
hgdprs1064793766
ensemblrs1064793766
gopubmedrs1064793766
geneviewrs1064793766
scholarrs1064793766
googlers1064793766
pharmgkbrs1064793766
gwascentralrs1064793766
openSNPrs1064793766
23andMers1064793766
23andMe allrs1064793766
SNPshotrs1064793766
SNPdbers1064793766
MSV3drs1064793766
GWAS Ctlgrs1064793766
Max Magnitude0
ClinVar
Risk rs1064793766(G;G)
Alt rs1064793766(G;G)
Reference Rs1064793766(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17119692A>C
CLNSRC
CLNACC RCV000479064.1,