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rs876658693

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658693(-;-)
Make rs876658693(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31219061
GeneNF1
is asnp
is mentioned by
dbSNPrs876658693
dbSNP (old)rs876658693
ClinGenrs876658693
ebirs876658693
HLIrs876658693
Exacrs876658693
Varsomers876658693
Maprs876658693
PheGenIrs876658693
Biobankrs876658693
1000 genomesrs876658693
hgdprs876658693
ensemblrs876658693
gopubmedrs876658693
geneviewrs876658693
scholarrs876658693
googlers876658693
pharmgkbrs876658693
gwascentralrs876658693
openSNPrs876658693
23andMers876658693
23andMe allrs876658693
SNP Nexus

SNPshotrs876658693
SNPdbers876658693
MSV3drs876658693
GWAS Ctlgrs876658693
Max Magnitude0
ClinVar
Risk rs876658693(-;-)
Alt rs876658693(-;-)
Reference Rs876658693(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.29546079delG
CLNSRC
CLNACC RCV000215553.1,