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rs786202023

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202023(C;T)
Make rs786202023(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31232083
GeneNF1
is asnp
is mentioned by
dbSNPrs786202023
ebirs786202023
HLIrs786202023
Exacrs786202023
Varsomers786202023
Maprs786202023
PheGenIrs786202023
hapmaprs786202023
1000 genomesrs786202023
hgdprs786202023
ensemblrs786202023
gopubmedrs786202023
geneviewrs786202023
scholarrs786202023
googlers786202023
pharmgkbrs786202023
gwascentralrs786202023
openSNPrs786202023
23andMers786202023
23andMe allrs786202023
SNP Nexus

SNPshotrs786202023
SNPdbers786202023
MSV3drs786202023
GWAS Ctlgrs786202023
Max Magnitude0
ClinVar
Risk rs786202023(T;T)
Alt rs786202023(T;T)
Reference rs786202023(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29559101C>T
CLNSRC
CLNACC RCV000164621.1,