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rs1060500331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500331(G;T)
Make rs1060500331(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31214586
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500331
dbSNP (old)rs1060500331
ClinGenrs1060500331
ebirs1060500331
HLIrs1060500331
Exacrs1060500331
Gnomadrs1060500331
Varsomers1060500331
Maprs1060500331
PheGenIrs1060500331
Biobankrs1060500331
1000 genomesrs1060500331
hgdprs1060500331
ensemblrs1060500331
gopubmedrs1060500331
geneviewrs1060500331
scholarrs1060500331
googlers1060500331
pharmgkbrs1060500331
gwascentralrs1060500331
openSNPrs1060500331
23andMers1060500331
23andMe allrs1060500331
SNPshotrs1060500331
SNPdbers1060500331
MSV3drs1060500331
GWAS Ctlgrs1060500331
Max Magnitude0
ClinVar
Risk rs1060500331(T;T)
Alt rs1060500331(T;T)
Reference Rs1060500331(G;G)
Significance Probable-Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29541604G>T
CLNSRC
CLNACC RCV000461603.1,