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rs267606608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267606608(-;-)
Make rs267606608(-;TG)
Make rs267606608(TG;TG)
ReferenceGRCh38 38.1/141
Chromosome17
Position31249104
GeneNF1
is asnp
is mentioned by
dbSNPrs267606608
ebirs267606608
HLIrs267606608
Exacrs267606608
Varsomers267606608
Maprs267606608
PheGenIrs267606608
hapmaprs267606608
1000 genomesrs267606608
hgdprs267606608
ensemblrs267606608
gopubmedrs267606608
geneviewrs267606608
scholarrs267606608
googlers267606608
pharmgkbrs267606608
gwascentralrs267606608
openSNPrs267606608
23andMers267606608
23andMe allrs267606608
SNP Nexus

SNPshotrs267606608
SNPdbers267606608
MSV3drs267606608
GWAS Ctlgrs267606608
Max Magnitude0
ClinVar
Risk rs267606608(TG;TG)
Alt rs267606608(TG;TG)
Reference rs267606608(;)
Significance Pathogenic
Disease Neurofibromatosis-Noonan syndrome
Variation info
Gene NF1
CLNDBN Neurofibromatosis-Noonan syndrome
Reversed 0
HGVS NC_000017.10:g.29576122_29576123insTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000395.3,