Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517848(A;G)
Make rs1057517848(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31227294
GeneNF1
is asnp
is mentioned by
dbSNPrs1057517848
dbSNP (old)rs1057517848
ClinGenrs1057517848
ebirs1057517848
HLIrs1057517848
Exacrs1057517848
Gnomadrs1057517848
Varsomers1057517848
LitVarrs1057517848
Maprs1057517848
PheGenIrs1057517848
Biobankrs1057517848
1000 genomesrs1057517848
hgdprs1057517848
ensemblrs1057517848
gopubmedrs1057517848
geneviewrs1057517848
scholarrs1057517848
googlers1057517848
pharmgkbrs1057517848
gwascentralrs1057517848
openSNPrs1057517848
23andMers1057517848
23andMe allrs1057517848
SNPshotrs1057517848
SNPdbers1057517848
MSV3drs1057517848
GWAS Ctlgrs1057517848
Max Magnitude0
ClinVar
Risk rs1057517848(G;G)
Alt rs1057517848(G;G)
Reference Rs1057517848(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene NF1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.29554312A>G
CLNSRC
CLNACC RCV000414580.1,