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rs769048538

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769048538(C;T)
Make rs769048538(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31181760
GeneNF1
is asnp
is mentioned by
dbSNPrs769048538
ebirs769048538
HLIrs769048538
Exacrs769048538
Varsomers769048538
Maprs769048538
PheGenIrs769048538
hapmaprs769048538
1000 genomesrs769048538
hgdprs769048538
ensemblrs769048538
gopubmedrs769048538
geneviewrs769048538
scholarrs769048538
googlers769048538
pharmgkbrs769048538
gwascentralrs769048538
openSNPrs769048538
23andMers769048538
23andMe allrs769048538
SNP Nexus

SNPshotrs769048538
SNPdbers769048538
MSV3drs769048538
GWAS Ctlgrs769048538
Max Magnitude0
ClinVar
Risk rs769048538(G,T;G,T)
Alt rs769048538(G,T;G,T)
Reference rs769048538(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29508778C>G
CLNSRC
CLNACC RCV000166611.1,