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rs74315496

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315496(C;T)
Make rs74315496(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position29661313
GeneNF2
is asnp
is mentioned by
dbSNPrs74315496
ebirs74315496
HLIrs74315496
Exacrs74315496
Varsomers74315496
Maprs74315496
PheGenIrs74315496
hapmaprs74315496
1000 genomesrs74315496
hgdprs74315496
ensemblrs74315496
gopubmedrs74315496
geneviewrs74315496
scholarrs74315496
googlers74315496
pharmgkbrs74315496
gwascentralrs74315496
openSNPrs74315496
23andMers74315496
23andMe allrs74315496
SNP Nexus

SNPshotrs74315496
SNPdbers74315496
MSV3drs74315496
GWAS Ctlgrs74315496
Max Magnitude0
OMIM607379
Desc
Variant0009
Relatedalso
ClinVar
Risk rs74315496(T;T)
Alt rs74315496(T;T)
Reference rs74315496(C;C)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF2
CLNDBN Neurofibromatosis, type 2
Reversed 0
HGVS NC_000022.10:g.30057302C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003451.2,