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rs587777177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777177(C;T)
Make rs587777177(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position20987548
GeneLZTR1
is asnp
is mentioned by
dbSNPrs587777177
dbSNP (classic)rs587777177
ClinGenrs587777177
ebirs587777177
HLIrs587777177
Exacrs587777177
Gnomadrs587777177
Varsomers587777177
LitVarrs587777177
Maprs587777177
PheGenIrs587777177
Biobankrs587777177
1000 genomesrs587777177
hgdprs587777177
ensemblrs587777177
geneviewrs587777177
scholarrs587777177
googlers587777177
pharmgkbrs587777177
gwascentralrs587777177
openSNPrs587777177
23andMers587777177
SNPshotrs587777177
SNPdbers587777177
MSV3drs587777177
GWAS Ctlgrs587777177
Max Magnitude0
ClinVar
Risk rs587777177(T;T)
Alt rs587777177(T;T)
Reference Rs587777177(C;C)
Significance Pathogenic
Disease Schwannomatosis 2
Variation info
Gene LZTR1
CLNDBN Schwannomatosis 2
Reversed 0
HGVS NC_000022.10:g.21341837C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000087293.4,