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rs199474747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 5.5 Neurofibromatosis type 1
(G;T) 5.5 Neurofibromatosis type 1
(T;T) 0 common in clinvar


Make rs199474747(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31229155
GeneNF1
is asnp
is mentioned by
dbSNPrs199474747
dbSNP (classic)rs199474747
ClinGenrs199474747
ebirs199474747
HLIrs199474747
Exacrs199474747
Gnomadrs199474747
Varsomers199474747
LitVarrs199474747
Maprs199474747
PheGenIrs199474747
Biobankrs199474747
1000 genomesrs199474747
hgdprs199474747
ensemblrs199474747
geneviewrs199474747
scholarrs199474747
googlers199474747
pharmgkbrs199474747
gwascentralrs199474747
openSNPrs199474747
23andMers199474747
SNPshotrs199474747
SNPdbers199474747
MSV3drs199474747
GWAS Ctlgrs199474747
Max Magnitude5.5

aka c.2540T>C or p.Leu847Pro, and also c.2540T>G or p.Leu847Arg

see NF1

ClinVar
Risk rs199474747(C;C)
Alt rs199474747(C;C)
Reference Rs199474747(T;T)
Significance Pathogenic
Disease not provided Neurofibromatosis Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN not provided Neurofibromatosis, type 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29556173T>C
CLNSRC UniProtKB (protein) UniProtKB (variants)
CLNACC RCV000059175.1, RCV000205919.2, RCV000492608.1,