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rs398123036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123036(C;T)
Make rs398123036(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position45516118
GeneLARS2
is asnp
is mentioned by
dbSNPrs398123036
ebirs398123036
HLIrs398123036
Exacrs398123036
Varsomers398123036
Maprs398123036
PheGenIrs398123036
hapmaprs398123036
1000 genomesrs398123036
hgdprs398123036
ensemblrs398123036
gopubmedrs398123036
geneviewrs398123036
scholarrs398123036
googlers398123036
pharmgkbrs398123036
gwascentralrs398123036
openSNPrs398123036
23andMers398123036
23andMe allrs398123036
SNP Nexus

SNPshotrs398123036
SNPdbers398123036
MSV3drs398123036
GWAS Ctlgrs398123036
Max Magnitude0
ClinVar
Risk rs398123036(T;T)
Alt rs398123036(T;T)
Reference rs398123036(C;C)
Significance Pathogenic
Disease Perrault syndrome 4
Variation info
Gene LARS2
CLNDBN Perrault syndrome 4
Reversed 0
HGVS NC_000003.11:g.45557610C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049286.4,