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rs794728682

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728682(A;A)
Make rs794728682(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position29661340
GeneNF2
is asnp
is mentioned by
dbSNPrs794728682
ebirs794728682
HLIrs794728682
Exacrs794728682
Varsomers794728682
Maprs794728682
PheGenIrs794728682
hapmaprs794728682
1000 genomesrs794728682
hgdprs794728682
ensemblrs794728682
gopubmedrs794728682
geneviewrs794728682
scholarrs794728682
googlers794728682
pharmgkbrs794728682
gwascentralrs794728682
openSNPrs794728682
23andMers794728682
23andMe allrs794728682
SNP Nexus

SNPshotrs794728682
SNPdbers794728682
MSV3drs794728682
GWAS Ctlgrs794728682
Max Magnitude0
ClinVar
Risk rs794728682(A;A)
Alt rs794728682(A;A)
Reference rs794728682(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NF2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.30057329G>A
CLNSRC
CLNACC RCV000182571.1,