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rs1057521097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521097(G;G)
Make rs1057521097(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31163208
GeneNF1
is asnp
is mentioned by
dbSNPrs1057521097
dbSNP (old)rs1057521097
ClinGenrs1057521097
ebirs1057521097
HLIrs1057521097
Exacrs1057521097
Gnomadrs1057521097
Varsomers1057521097
LitVarrs1057521097
Maprs1057521097
PheGenIrs1057521097
Biobankrs1057521097
1000 genomesrs1057521097
hgdprs1057521097
ensemblrs1057521097
gopubmedrs1057521097
geneviewrs1057521097
scholarrs1057521097
googlers1057521097
pharmgkbrs1057521097
gwascentralrs1057521097
openSNPrs1057521097
23andMers1057521097
23andMe allrs1057521097
SNPshotrs1057521097
SNPdbers1057521097
MSV3drs1057521097
GWAS Ctlgrs1057521097
Max Magnitude0
ClinVar
Risk rs1057521097(G;G)
Alt rs1057521097(G;G)
Reference Rs1057521097(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NF1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.29490226T>G
CLNSRC
CLNACC RCV000424712.1,