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rs1064794276

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TGTT;TGTT) 0 common in clinvar
Chromosome17
Position31235641
GeneNF1
is asnp
is mentioned by
dbSNPrs1064794276
dbSNP (old)rs1064794276
ClinGenrs1064794276
ebirs1064794276
HLIrs1064794276
Exacrs1064794276
Gnomadrs1064794276
Varsomers1064794276
Maprs1064794276
PheGenIrs1064794276
Biobankrs1064794276
1000 genomesrs1064794276
hgdprs1064794276
ensemblrs1064794276
gopubmedrs1064794276
geneviewrs1064794276
scholarrs1064794276
googlers1064794276
pharmgkbrs1064794276
gwascentralrs1064794276
openSNPrs1064794276
23andMers1064794276
23andMe allrs1064794276
SNPshotrs1064794276
SNPdbers1064794276
MSV3drs1064794276
GWAS Ctlgrs1064794276
Max Magnitude0
ClinVar
Risk rs1064794276(-;-)
Alt rs1064794276(-;-)
Reference Rs1064794276(TGTT;TGTT)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29562659_29562662delTTTG
CLNSRC
CLNACC RCV000482277.1, RCV000492776.1,