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rs74315498

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315498(C;T)
Make rs74315498(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position29671910
GeneNF2
is asnp
is mentioned by
dbSNPrs74315498
ebirs74315498
HLIrs74315498
Exacrs74315498
Varsomers74315498
Maprs74315498
PheGenIrs74315498
hapmaprs74315498
1000 genomesrs74315498
hgdprs74315498
ensemblrs74315498
gopubmedrs74315498
geneviewrs74315498
scholarrs74315498
googlers74315498
pharmgkbrs74315498
gwascentralrs74315498
openSNPrs74315498
23andMers74315498
23andMe allrs74315498
SNP Nexus

SNPshotrs74315498
SNPdbers74315498
MSV3drs74315498
GWAS Ctlgrs74315498
Max Magnitude0
OMIM607379
Desc
Variant0010
Relatedalso
ClinVar
Risk rs74315498(T;T)
Alt rs74315498(T;T)
Reference rs74315498(C;C)
Significance Untested
Disease Neurofibromatosis
Variation info
Gene NF2
CLNDBN Neurofibromatosis, type 2
Reversed 0
HGVS NC_000022.10:g.30067899C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000023610.1, SCV000023610.1,