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rs74315495

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315495(G;T)
Make rs74315495(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position29655621
GeneNF2
is asnp
is mentioned by
dbSNPrs74315495
ClinGenrs74315495
ebirs74315495
HLIrs74315495
Exacrs74315495
Varsomers74315495
Maprs74315495
PheGenIrs74315495
hapmaprs74315495
1000 genomesrs74315495
hgdprs74315495
ensemblrs74315495
gopubmedrs74315495
geneviewrs74315495
scholarrs74315495
googlers74315495
pharmgkbrs74315495
gwascentralrs74315495
openSNPrs74315495
23andMers74315495
23andMe allrs74315495
SNP Nexus

SNPshotrs74315495
SNPdbers74315495
MSV3drs74315495
GWAS Ctlgrs74315495
Max Magnitude0
OMIM607379
Desc
Variant0008
Relatedalso
ClinVar
Risk rs74315495(T;T)
Alt rs74315495(T;T)
Reference Rs74315495(G;G)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF2
CLNDBN Neurofibromatosis, type 2
Reversed 0
HGVS NC_000022.10:g.30051610G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003450.2,