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rs1064793127

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position17227884
GeneFLCN
is asnp
is mentioned by
dbSNPrs1064793127
dbSNP (old)rs1064793127
ClinGenrs1064793127
ebirs1064793127
HLIrs1064793127
Exacrs1064793127
Gnomadrs1064793127
Varsomers1064793127
Maprs1064793127
PheGenIrs1064793127
Biobankrs1064793127
1000 genomesrs1064793127
hgdprs1064793127
ensemblrs1064793127
gopubmedrs1064793127
geneviewrs1064793127
scholarrs1064793127
googlers1064793127
pharmgkbrs1064793127
gwascentralrs1064793127
openSNPrs1064793127
23andMers1064793127
23andMe allrs1064793127
SNPshotrs1064793127
SNPdbers1064793127
MSV3drs1064793127
GWAS Ctlgrs1064793127
Max Magnitude0
ClinVar
Risk rs1064793127(A;A)
Alt rs1064793127(A;A)
Reference Rs1064793127(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17131198C>T
CLNSRC
CLNACC RCV000485638.1,