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

rs199474737

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199474737(C;C)
Make rs199474737(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31219072
GeneNF1
is asnp
is mentioned by
dbSNPrs199474737
ebirs199474737
HLIrs199474737
Exacrs199474737
Varsomers199474737
Maprs199474737
PheGenIrs199474737
hapmaprs199474737
1000 genomesrs199474737
hgdprs199474737
ensemblrs199474737
gopubmedrs199474737
geneviewrs199474737
scholarrs199474737
googlers199474737
pharmgkbrs199474737
gwascentralrs199474737
openSNPrs199474737
23andMers199474737
23andMe allrs199474737
SNP Nexus

SNPshotrs199474737
SNPdbers199474737
MSV3drs199474737
GWAS Ctlgrs199474737
Max Magnitude0
ClinVar
Risk rs199474737(C,G;C,G)
Alt rs199474737(C,G;C,G)
Reference rs199474737(T;T)
Significance Pathogenic
Disease not provided Neurofibromatosis
Variation info
Gene NF1
CLNDBN not provided Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29546090T>C; NC_000017.10:g.29546090T>G
CLNSRC UniProtKB (variants)
CLNACC RCV000059154.1, RCV000168173.1, RCV000227710.1,