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rs876659964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs876659964(-;T)
Make rs876659964(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31258436
GeneNF1
is asnp
is mentioned by
dbSNPrs876659964
dbSNP (old)rs876659964
ClinGenrs876659964
ebirs876659964
HLIrs876659964
Exacrs876659964
Gnomadrs876659964
Varsomers876659964
Maprs876659964
PheGenIrs876659964
Biobankrs876659964
1000 genomesrs876659964
hgdprs876659964
ensemblrs876659964
gopubmedrs876659964
geneviewrs876659964
scholarrs876659964
googlers876659964
pharmgkbrs876659964
gwascentralrs876659964
openSNPrs876659964
23andMers876659964
23andMe allrs876659964
SNP Nexus

SNPshotrs876659964
SNPdbers876659964
MSV3drs876659964
GWAS Ctlgrs876659964
Max Magnitude0
ClinVar
Risk rs876659964(T;T)
Alt rs876659964(T;T)
Reference Rs876659964(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29585454dupT
CLNSRC
CLNACC RCV000218073.1,