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rs786202954

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202954(-;-)
Make rs786202954(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31226611
GeneNF1
is asnp
is mentioned by
dbSNPrs786202954
ebirs786202954
HLIrs786202954
Exacrs786202954
Varsomers786202954
Maprs786202954
PheGenIrs786202954
hapmaprs786202954
1000 genomesrs786202954
hgdprs786202954
ensemblrs786202954
gopubmedrs786202954
geneviewrs786202954
scholarrs786202954
googlers786202954
pharmgkbrs786202954
gwascentralrs786202954
openSNPrs786202954
23andMers786202954
23andMe allrs786202954
SNP Nexus

SNPshotrs786202954
SNPdbers786202954
MSV3drs786202954
GWAS Ctlgrs786202954
Max Magnitude0
ClinVar
Risk rs786202954(;)
Alt rs786202954(;)
Reference rs786202954(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29553629delG
CLNSRC
CLNACC RCV000166034.1,