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

rs199474786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199474786(C;C)
Make rs199474786(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position31229308
GeneNF1
is asnp
is mentioned by
dbSNPrs199474786
ebirs199474786
HLIrs199474786
Exacrs199474786
Varsomers199474786
Maprs199474786
PheGenIrs199474786
hapmaprs199474786
1000 genomesrs199474786
hgdprs199474786
ensemblrs199474786
gopubmedrs199474786
geneviewrs199474786
scholarrs199474786
googlers199474786
pharmgkbrs199474786
gwascentralrs199474786
openSNPrs199474786
23andMers199474786
23andMe allrs199474786
SNP Nexus

SNPshotrs199474786
SNPdbers199474786
MSV3drs199474786
GWAS Ctlgrs199474786
Max Magnitude0
ClinVar
Risk rs199474786(C;C)
Alt rs199474786(C;C)
Reference rs199474786(T;T)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29556326T>C
CLNSRC UniProtKB (variants)
CLNACC RCV000059178.1, RCV000129792.2,