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rs786204251

From SNPedia

Orientationplus
Geno Mag Summary
(ACTC;ACTC) 0 common in clinvar
Make rs786204251(-;-)
Make rs786204251(-;ACTC)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31232841
GeneNF1
is asnp
is mentioned by
dbSNPrs786204251
ebirs786204251
HLIrs786204251
Exacrs786204251
Varsomers786204251
Maprs786204251
PheGenIrs786204251
hapmaprs786204251
1000 genomesrs786204251
hgdprs786204251
ensemblrs786204251
gopubmedrs786204251
geneviewrs786204251
scholarrs786204251
googlers786204251
pharmgkbrs786204251
gwascentralrs786204251
openSNPrs786204251
23andMers786204251
23andMe allrs786204251
SNP Nexus

SNPshotrs786204251
SNPdbers786204251
MSV3drs786204251
GWAS Ctlgrs786204251
Max Magnitude0
ClinVar
Risk rs786204251(;)
Alt rs786204251(;)
Reference rs786204251(ACTC;ACTC)
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.29559860_29559863delCTCA
CLNSRC
CLNACC RCV000165479.1, RCV000168453.1,