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rs786203448

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203448(C;T)
Make rs786203448(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31181460
GeneNF1
is asnp
is mentioned by
dbSNPrs786203448
ebirs786203448
HLIrs786203448
Exacrs786203448
Varsomers786203448
Maprs786203448
PheGenIrs786203448
hapmaprs786203448
1000 genomesrs786203448
hgdprs786203448
ensemblrs786203448
gopubmedrs786203448
geneviewrs786203448
scholarrs786203448
googlers786203448
pharmgkbrs786203448
gwascentralrs786203448
openSNPrs786203448
23andMers786203448
23andMe allrs786203448
SNP Nexus

SNPshotrs786203448
SNPdbers786203448
MSV3drs786203448
GWAS Ctlgrs786203448
Max Magnitude0
ClinVar
Risk rs786203448(T;T)
Alt rs786203448(T;T)
Reference rs786203448(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Neurofibromatosis
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29508478C>T
CLNSRC
CLNACC RCV000166757.1, RCV000204041.1,