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rs267606607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
(GAA;GAA) 0 common in clinvar
Make rs267606607(-;-)
Make rs267606607(-;GAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position31259074
GeneNF1
is asnp
is mentioned by
dbSNPrs267606607
ebirs267606607
HLIrs267606607
Exacrs267606607
Varsomers267606607
Maprs267606607
PheGenIrs267606607
hapmaprs267606607
1000 genomesrs267606607
hgdprs267606607
ensemblrs267606607
gopubmedrs267606607
geneviewrs267606607
scholarrs267606607
googlers267606607
pharmgkbrs267606607
gwascentralrs267606607
openSNPrs267606607
23andMers267606607
23andMe allrs267606607
SNP Nexus

SNPshotrs267606607
SNPdbers267606607
MSV3drs267606607
GWAS Ctlgrs267606607
Max Magnitude0
ClinVar
Risk rs267606607(;)
Alt rs267606607(;)
Reference rs267606607(AAG;AAG)
Significance Pathogenic
Disease Neurofibromatosis-Noonan syndrome
Variation info
Gene NF1
CLNDBN Neurofibromatosis-Noonan syndrome
Reversed 0
HGVS NC_000017.10:g.29586092_29586094delGAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000394.3,