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rs786201874

From SNPedia

Orientationplus
Geno Mag Summary
(TGTT;TGTT) 0 common in clinvar
Make rs786201874(-;-)
Make rs786201874(-;TGTT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31169910
GeneNF1
is asnp
is mentioned by
dbSNPrs786201874
ebirs786201874
HLIrs786201874
Exacrs786201874
Varsomers786201874
Maprs786201874
PheGenIrs786201874
hapmaprs786201874
1000 genomesrs786201874
hgdprs786201874
ensemblrs786201874
gopubmedrs786201874
geneviewrs786201874
scholarrs786201874
googlers786201874
pharmgkbrs786201874
gwascentralrs786201874
openSNPrs786201874
23andMers786201874
23andMe allrs786201874
SNP Nexus

SNPshotrs786201874
SNPdbers786201874
MSV3drs786201874
GWAS Ctlgrs786201874
Max Magnitude0
ClinVar
Risk rs786201874(;)
Alt rs786201874(;)
Reference rs786201874(TGTT;TGTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29496928_29496931delTGTT
CLNSRC
CLNACC RCV000164374.1,