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rs876660931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs876660931(-;A)
Make rs876660931(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31200488
GeneNF1
is asnp
is mentioned by
dbSNPrs876660931
dbSNP (classic)rs876660931
ClinGenrs876660931
ebirs876660931
HLIrs876660931
Exacrs876660931
Gnomadrs876660931
Varsomers876660931
LitVarrs876660931
Maprs876660931
PheGenIrs876660931
Biobankrs876660931
1000 genomesrs876660931
hgdprs876660931
ensemblrs876660931
geneviewrs876660931
scholarrs876660931
googlers876660931
pharmgkbrs876660931
gwascentralrs876660931
openSNPrs876660931
23andMers876660931
SNPshotrs876660931
SNPdbers876660931
MSV3drs876660931
GWAS Ctlgrs876660931
Max Magnitude0
ClinVar
Risk rs876660931(A;A)
Alt rs876660931(A;A)
Reference Rs876660931(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29527506dupA
CLNSRC
CLNACC RCV000219150.1,