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rs1060500374

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060500374(A;A)
Make rs1060500374(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31233128
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500374
dbSNP (old)rs1060500374
ClinGenrs1060500374
ebirs1060500374
HLIrs1060500374
Exacrs1060500374
Gnomadrs1060500374
Varsomers1060500374
Maprs1060500374
PheGenIrs1060500374
Biobankrs1060500374
1000 genomesrs1060500374
hgdprs1060500374
ensemblrs1060500374
gopubmedrs1060500374
geneviewrs1060500374
scholarrs1060500374
googlers1060500374
pharmgkbrs1060500374
gwascentralrs1060500374
openSNPrs1060500374
23andMers1060500374
23andMe allrs1060500374
SNPshotrs1060500374
SNPdbers1060500374
MSV3drs1060500374
GWAS Ctlgrs1060500374
Max Magnitude0
ClinVar
Risk rs1060500374(A;A)
Alt rs1060500374(A;A)
Reference Rs1060500374(T;T)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29560146T>A
CLNSRC
CLNACC RCV000460448.1,