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rs797044942

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044942(C;T)
Make rs797044942(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31265233
GeneNF1
is asnp
is mentioned by
dbSNPrs797044942
ebirs797044942
HLIrs797044942
Exacrs797044942
Varsomers797044942
Maprs797044942
PheGenIrs797044942
hapmaprs797044942
1000 genomesrs797044942
hgdprs797044942
ensemblrs797044942
gopubmedrs797044942
geneviewrs797044942
scholarrs797044942
googlers797044942
pharmgkbrs797044942
gwascentralrs797044942
openSNPrs797044942
23andMers797044942
23andMe allrs797044942
SNP Nexus

SNPshotrs797044942
SNPdbers797044942
MSV3drs797044942
GWAS Ctlgrs797044942
Max Magnitude0
ClinVar
Risk rs797044942(T;T)
Alt rs797044942(T;T)
Reference rs797044942(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NF1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000017.10:g.29592251C>T
CLNSRC
CLNACC RCV000190788.1,