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rs767671406

From SNPedia

Orientationplus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs767671406(-;-)
Make rs767671406(-;GAG)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17216506
GeneFLCN
is asnp
is mentioned by
dbSNPrs767671406
ebirs767671406
HLIrs767671406
Exacrs767671406
Varsomers767671406
Maprs767671406
PheGenIrs767671406
hapmaprs767671406
1000 genomesrs767671406
hgdprs767671406
ensemblrs767671406
gopubmedrs767671406
geneviewrs767671406
scholarrs767671406
googlers767671406
pharmgkbrs767671406
gwascentralrs767671406
openSNPrs767671406
23andMers767671406
23andMe allrs767671406
SNP Nexus

SNPshotrs767671406
SNPdbers767671406
MSV3drs767671406
GWAS Ctlgrs767671406
Max Magnitude0
ClinVar
Risk rs767671406(;)
Alt rs767671406(;)
Reference rs767671406(GAG;GAG)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not specified Multiple fibrofolliculomas
Variation info
Gene FLCN LOC101928660
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not specified Multiple fibrofolliculomas
Reversed 0
HGVS NC_000017.10:g.17119820_17119822delGAG
CLNSRC
CLNACC RCV000217238.1, RCV000217604.1, RCV000239690.1,