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rs786203950

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203950(C;T)
Make rs786203950(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31200443
GeneNF1
is asnp
is mentioned by
dbSNPrs786203950
ebirs786203950
HLIrs786203950
Exacrs786203950
Varsomers786203950
Maprs786203950
PheGenIrs786203950
hapmaprs786203950
1000 genomesrs786203950
hgdprs786203950
ensemblrs786203950
gopubmedrs786203950
geneviewrs786203950
scholarrs786203950
googlers786203950
pharmgkbrs786203950
gwascentralrs786203950
openSNPrs786203950
23andMers786203950
23andMe allrs786203950
SNP Nexus

SNPshotrs786203950
SNPdbers786203950
MSV3drs786203950
GWAS Ctlgrs786203950
Max Magnitude0
ClinVar
Risk rs786203950(T;T)
Alt rs786203950(T;T)
Reference rs786203950(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.29527461C>T
CLNSRC
CLNACC RCV000167474.1,