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rs587777613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777613(-;-)
Make rs587777613(-;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position20982398
GeneLZTR1
is asnp
is mentioned by
dbSNPrs587777613
dbSNP (classic)rs587777613
ClinGenrs587777613
ebirs587777613
HLIrs587777613
Exacrs587777613
Gnomadrs587777613
Varsomers587777613
LitVarrs587777613
Maprs587777613
PheGenIrs587777613
Biobankrs587777613
1000 genomesrs587777613
hgdprs587777613
ensemblrs587777613
geneviewrs587777613
scholarrs587777613
googlers587777613
pharmgkbrs587777613
gwascentralrs587777613
openSNPrs587777613
23andMers587777613
SNPshotrs587777613
SNPdbers587777613
MSV3drs587777613
GWAS Ctlgrs587777613
Max Magnitude0
ClinVar
Risk rs587777613(-;-)
Alt rs587777613(-;-)
Reference Rs587777613(G;G)
Significance Pathogenic
Disease Schwannomatosis 2
Variation info
Gene LZTR1
CLNDBN Schwannomatosis 2
Reversed 0
HGVS NC_000022.10:g.21336687delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000133460.2,