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

rs267606597

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs267606597(-;T)
Make rs267606597(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position31327758
GeneNF1
is asnp
is mentioned by
dbSNPrs267606597
dbSNP (classic)rs267606597
ClinGenrs267606597
ebirs267606597
HLIrs267606597
Exacrs267606597
Gnomadrs267606597
Varsomers267606597
LitVarrs267606597
Maprs267606597
PheGenIrs267606597
Biobankrs267606597
1000 genomesrs267606597
hgdprs267606597
ensemblrs267606597
geneviewrs267606597
scholarrs267606597
googlers267606597
pharmgkbrs267606597
gwascentralrs267606597
openSNPrs267606597
23andMers267606597
SNPshotrs267606597
SNPdbers267606597
MSV3drs267606597
GWAS Ctlgrs267606597
Max Magnitude0
ClinVar
Risk rs267606597(T;T)
Alt rs267606597(T;T)
Reference Rs267606597(-;-)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29654776_29654777insT
CLNSRC OMIM Allelic Variant
CLNACC RCV000000366.3,