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rs797045166

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045166(A;A)
Make rs797045166(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position20990474
GeneLZTR1
is asnp
is mentioned by
dbSNPrs797045166
ebirs797045166
HLIrs797045166
Exacrs797045166
Varsomers797045166
Maprs797045166
PheGenIrs797045166
hapmaprs797045166
1000 genomesrs797045166
hgdprs797045166
ensemblrs797045166
gopubmedrs797045166
geneviewrs797045166
scholarrs797045166
googlers797045166
pharmgkbrs797045166
gwascentralrs797045166
openSNPrs797045166
23andMers797045166
23andMe allrs797045166
SNP Nexus

SNPshotrs797045166
SNPdbers797045166
MSV3drs797045166
GWAS Ctlgrs797045166
Max Magnitude0
ClinVar
Risk rs797045166(A;A)
Alt rs797045166(A;A)
Reference rs797045166(G;G)
Significance Pathogenic
Disease Noonan syndrome 10
Variation info
Gene LZTR1
CLNDBN Noonan syndrome 10
Reversed 0
HGVS NC_000022.10:g.21344763G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000191029.2,