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rs1060500355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500355(A;A)
Make rs1060500355(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31338806
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500355
dbSNP (classic)rs1060500355
ClinGenrs1060500355
ebirs1060500355
HLIrs1060500355
Exacrs1060500355
Gnomadrs1060500355
Varsomers1060500355
LitVarrs1060500355
Maprs1060500355
PheGenIrs1060500355
Biobankrs1060500355
1000 genomesrs1060500355
hgdprs1060500355
ensemblrs1060500355
geneviewrs1060500355
scholarrs1060500355
googlers1060500355
pharmgkbrs1060500355
gwascentralrs1060500355
openSNPrs1060500355
23andMers1060500355
23andMe allrs1060500355
SNPshotrs1060500355
SNPdbers1060500355
MSV3drs1060500355
GWAS Ctlgrs1060500355
Max Magnitude0
ClinVar
Risk rs1060500355(A;A)
Alt rs1060500355(A;A)
Reference Rs1060500355(G;G)
Significance Probable-Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29665824G>A
CLNSRC
CLNACC RCV000476980.1,