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rs1057518147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs1057518147(-;-)
Make rs1057518147(-;AT)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17227896
GeneFLCN
is asnp
is mentioned by
dbSNPrs1057518147
dbSNP (classic)rs1057518147
ClinGenrs1057518147
ebirs1057518147
HLIrs1057518147
Exacrs1057518147
Gnomadrs1057518147
Varsomers1057518147
LitVarrs1057518147
Maprs1057518147
PheGenIrs1057518147
Biobankrs1057518147
1000 genomesrs1057518147
hgdprs1057518147
ensemblrs1057518147
geneviewrs1057518147
scholarrs1057518147
googlers1057518147
pharmgkbrs1057518147
gwascentralrs1057518147
openSNPrs1057518147
23andMers1057518147
23andMe allrs1057518147
SNPshotrs1057518147
SNPdbers1057518147
MSV3drs1057518147
GWAS Ctlgrs1057518147
Max Magnitude0
ClinVar
Risk rs1057518147(-;-)
Alt rs1057518147(-;-)
Reference Rs1057518147(AT;AT)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17131210_17131211delAT
CLNSRC
CLNACC RCV000413452.1,