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rs1060499999

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499999(A;A)
Make rs1060499999(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position9787633
GeneSBF2, SBF2-AS1
is asnp
is mentioned by
dbSNPrs1060499999
dbSNP (old)rs1060499999
ClinGenrs1060499999
ebirs1060499999
HLIrs1060499999
Exacrs1060499999
Gnomadrs1060499999
Varsomers1060499999
Maprs1060499999
PheGenIrs1060499999
Biobankrs1060499999
1000 genomesrs1060499999
hgdprs1060499999
ensemblrs1060499999
gopubmedrs1060499999
geneviewrs1060499999
scholarrs1060499999
googlers1060499999
pharmgkbrs1060499999
gwascentralrs1060499999
openSNPrs1060499999
23andMers1060499999
23andMe allrs1060499999
SNPshotrs1060499999
SNPdbers1060499999
MSV3drs1060499999
GWAS Ctlgrs1060499999
Max Magnitude0
ClinVar
Risk rs1060499999(A;A)
Alt rs1060499999(A;A)
Reference Rs1060499999(G;G)
Significance Probable-Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene SBF2 SBF2-AS1
CLNDBN Charcot-Marie-Tooth disease, type IV
Reversed 1
HGVS NC_000011.9:g.9809180C>T
CLNSRC
CLNACC RCV000471492.1,