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rs786203307

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203307(G;T)
Make rs786203307(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31095364
GeneLOC105371722, MIR4733, NF1
is asnp
is mentioned by
dbSNPrs786203307
ebirs786203307
HLIrs786203307
Exacrs786203307
Varsomers786203307
Maprs786203307
PheGenIrs786203307
hapmaprs786203307
1000 genomesrs786203307
hgdprs786203307
ensemblrs786203307
gopubmedrs786203307
geneviewrs786203307
scholarrs786203307
googlers786203307
pharmgkbrs786203307
gwascentralrs786203307
openSNPrs786203307
23andMers786203307
23andMe allrs786203307
SNP Nexus

SNPshotrs786203307
SNPdbers786203307
MSV3drs786203307
GWAS Ctlgrs786203307
Max Magnitude0
ClinVar
Risk rs786203307(T;T)
Alt rs786203307(T;T)
Reference rs786203307(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1 MIR4733
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29422382G>T
CLNSRC
CLNACC RCV000166554.1,