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rs1064795492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTCC;CTCC) 0 common in clinvar
Chromosome17
Position31336837
GeneNF1
is asnp
is mentioned by
dbSNPrs1064795492
dbSNP (old)rs1064795492
ClinGenrs1064795492
ebirs1064795492
HLIrs1064795492
Exacrs1064795492
Gnomadrs1064795492
Varsomers1064795492
Maprs1064795492
PheGenIrs1064795492
Biobankrs1064795492
1000 genomesrs1064795492
hgdprs1064795492
ensemblrs1064795492
gopubmedrs1064795492
geneviewrs1064795492
scholarrs1064795492
googlers1064795492
pharmgkbrs1064795492
gwascentralrs1064795492
openSNPrs1064795492
23andMers1064795492
23andMe allrs1064795492
SNPshotrs1064795492
SNPdbers1064795492
MSV3drs1064795492
GWAS Ctlgrs1064795492
Max Magnitude0
ClinVar
Risk rs1064795492(-;-)
Alt rs1064795492(-;-)
Reference Rs1064795492(CTCC;CTCC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NF1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.29663855_29663858delCCCT
CLNSRC
CLNACC RCV000481849.1,