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rs786203614

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203614(-;-)
Make rs786203614(-;T)
Make rs786203614(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31235723
GeneNF1
is asnp
is mentioned by
dbSNPrs786203614
ebirs786203614
HLIrs786203614
Exacrs786203614
Varsomers786203614
Maprs786203614
PheGenIrs786203614
hapmaprs786203614
1000 genomesrs786203614
hgdprs786203614
ensemblrs786203614
gopubmedrs786203614
geneviewrs786203614
scholarrs786203614
googlers786203614
pharmgkbrs786203614
gwascentralrs786203614
openSNPrs786203614
23andMers786203614
23andMe allrs786203614
SNP Nexus

SNPshotrs786203614
SNPdbers786203614
MSV3drs786203614
GWAS Ctlgrs786203614
Max Magnitude0
ClinVar
Risk rs786203614(T;T)
Alt rs786203614(T;T)
Reference rs786203614(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29562741dupT
CLNSRC
CLNACC RCV000167004.1,