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rs1057520528

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520528(A;G)
Make rs1057520528(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17216505
GeneFLCN
is asnp
is mentioned by
dbSNPrs1057520528
dbSNP (old)rs1057520528
ClinGenrs1057520528
ebirs1057520528
HLIrs1057520528
Exacrs1057520528
Gnomadrs1057520528
Varsomers1057520528
Maprs1057520528
PheGenIrs1057520528
Biobankrs1057520528
1000 genomesrs1057520528
hgdprs1057520528
ensemblrs1057520528
gopubmedrs1057520528
geneviewrs1057520528
scholarrs1057520528
googlers1057520528
pharmgkbrs1057520528
gwascentralrs1057520528
openSNPrs1057520528
23andMers1057520528
23andMe allrs1057520528
SNPshotrs1057520528
SNPdbers1057520528
MSV3drs1057520528
GWAS Ctlgrs1057520528
Max Magnitude0
ClinVar
Risk rs1057520528(G;G)
Alt rs1057520528(G;G)
Reference Rs1057520528(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17119819T>C
CLNSRC
CLNACC RCV000444206.1,