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rs786203896

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203896(G;T)
Make rs786203896(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31330468
GeneNF1
is asnp
is mentioned by
dbSNPrs786203896
ebirs786203896
HLIrs786203896
Exacrs786203896
Varsomers786203896
Maprs786203896
PheGenIrs786203896
hapmaprs786203896
1000 genomesrs786203896
hgdprs786203896
ensemblrs786203896
gopubmedrs786203896
geneviewrs786203896
scholarrs786203896
googlers786203896
pharmgkbrs786203896
gwascentralrs786203896
openSNPrs786203896
23andMers786203896
23andMe allrs786203896
SNP Nexus

SNPshotrs786203896
SNPdbers786203896
MSV3drs786203896
GWAS Ctlgrs786203896
Max Magnitude0
ClinVar
Risk rs786203896(T;T)
Alt rs786203896(T;T)
Reference rs786203896(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29657486G>T
CLNSRC
CLNACC RCV000167400.1,