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rs886040871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886040871(-;AG)
Make rs886040871(AG;AG)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position50776244
GeneCYLD
is asnp
is mentioned by
dbSNPrs886040871
dbSNP (classic)rs886040871
ClinGenrs886040871
ebirs886040871
HLIrs886040871
Exacrs886040871
Gnomadrs886040871
Varsomers886040871
LitVarrs886040871
Maprs886040871
PheGenIrs886040871
Biobankrs886040871
1000 genomesrs886040871
hgdprs886040871
ensemblrs886040871
geneviewrs886040871
scholarrs886040871
googlers886040871
pharmgkbrs886040871
gwascentralrs886040871
openSNPrs886040871
23andMers886040871
SNPshotrs886040871
SNPdbers886040871
MSV3drs886040871
GWAS Ctlgrs886040871
Max Magnitude0
ClinVar
Risk rs886040871(AG;AG)
Alt rs886040871(AG;AG)
Reference Rs886040871(-;-)
Significance Pathogenic
Disease Cylindromatosis
Variation info
Gene CYLD
CLNDBN Cylindromatosis, familial
Reversed 0
HGVS NC_000016.9:g.50810154_50810155dupAG
CLNSRC
CLNACC RCV000257964.1,