Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517967

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517967(A;A)
Make rs1057517967(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31181724
GeneNF1
is asnp
is mentioned by
dbSNPrs1057517967
dbSNP (old)rs1057517967
ClinGenrs1057517967
ebirs1057517967
HLIrs1057517967
Exacrs1057517967
Gnomadrs1057517967
Varsomers1057517967
Maprs1057517967
PheGenIrs1057517967
Biobankrs1057517967
1000 genomesrs1057517967
hgdprs1057517967
ensemblrs1057517967
gopubmedrs1057517967
geneviewrs1057517967
scholarrs1057517967
googlers1057517967
pharmgkbrs1057517967
gwascentralrs1057517967
openSNPrs1057517967
23andMers1057517967
23andMe allrs1057517967
SNPshotrs1057517967
SNPdbers1057517967
MSV3drs1057517967
GWAS Ctlgrs1057517967
Max Magnitude0
ClinVar
Risk rs1057517967(A;A)
Alt rs1057517967(A;A)
Reference Rs1057517967(G;G)
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.29508742G>A
CLNSRC
CLNACC RCV000413819.1, RCV000492355.1,