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rs1057521098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521098(A;G)
Make rs1057521098(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31200598
GeneNF1
is asnp
is mentioned by
dbSNPrs1057521098
dbSNP (old)rs1057521098
ClinGenrs1057521098
ebirs1057521098
HLIrs1057521098
Exacrs1057521098
Gnomadrs1057521098
Varsomers1057521098
Maprs1057521098
PheGenIrs1057521098
Biobankrs1057521098
1000 genomesrs1057521098
hgdprs1057521098
ensemblrs1057521098
gopubmedrs1057521098
geneviewrs1057521098
scholarrs1057521098
googlers1057521098
pharmgkbrs1057521098
gwascentralrs1057521098
openSNPrs1057521098
23andMers1057521098
23andMe allrs1057521098
SNPshotrs1057521098
SNPdbers1057521098
MSV3drs1057521098
GWAS Ctlgrs1057521098
Max Magnitude0
ClinVar
Risk rs1057521098(G;G)
Alt rs1057521098(G;G)
Reference Rs1057521098(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NF1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.29527616A>G
CLNSRC
CLNACC RCV000437730.1,