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rs74315500

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315500(C;T)
Make rs74315500(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position29668417
GeneNF2
is asnp
is mentioned by
dbSNPrs74315500
ebirs74315500
HLIrs74315500
Exacrs74315500
Varsomers74315500
Maprs74315500
PheGenIrs74315500
hapmaprs74315500
1000 genomesrs74315500
hgdprs74315500
ensemblrs74315500
gopubmedrs74315500
geneviewrs74315500
scholarrs74315500
googlers74315500
pharmgkbrs74315500
gwascentralrs74315500
openSNPrs74315500
23andMers74315500
23andMe allrs74315500
SNP Nexus

SNPshotrs74315500
SNPdbers74315500
MSV3drs74315500
GWAS Ctlgrs74315500
Max Magnitude0
OMIM607379
Desc
Variant0012
Relatedalso
ClinVar
Risk rs74315500(T;T)
Alt rs74315500(T;T)
Reference rs74315500(C;C)
Significance Untested
Disease Neurofibromatosis
Variation info
Gene NF2
CLNDBN Neurofibromatosis, type 2
Reversed 0
HGVS NC_000022.10:g.30064406C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000023612.1, SCV000023612.1,