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rs1057521848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521848(G;T)
Make rs1057521848(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31233116
GeneNF1
is asnp
is mentioned by
dbSNPrs1057521848
dbSNP (old)rs1057521848
ClinGenrs1057521848
ebirs1057521848
HLIrs1057521848
Exacrs1057521848
Gnomadrs1057521848
Varsomers1057521848
LitVarrs1057521848
Maprs1057521848
PheGenIrs1057521848
Biobankrs1057521848
1000 genomesrs1057521848
hgdprs1057521848
ensemblrs1057521848
gopubmedrs1057521848
geneviewrs1057521848
scholarrs1057521848
googlers1057521848
pharmgkbrs1057521848
gwascentralrs1057521848
openSNPrs1057521848
23andMers1057521848
23andMe allrs1057521848
SNPshotrs1057521848
SNPdbers1057521848
MSV3drs1057521848
GWAS Ctlgrs1057521848
Max Magnitude0
ClinVar
Risk rs1057521848(T;T)
Alt rs1057521848(T;T)
Reference Rs1057521848(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NF1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.29560134G>T
CLNSRC
CLNACC RCV000425910.1,