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rs879255408

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255408(C;T)
Make rs879255408(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position45520267
GeneLARS2
is asnp
is mentioned by
dbSNPrs879255408
ebirs879255408
HLIrs879255408
Exacrs879255408
Varsomers879255408
Maprs879255408
PheGenIrs879255408
hapmaprs879255408
1000 genomesrs879255408
hgdprs879255408
ensemblrs879255408
gopubmedrs879255408
geneviewrs879255408
scholarrs879255408
googlers879255408
pharmgkbrs879255408
gwascentralrs879255408
openSNPrs879255408
23andMers879255408
23andMe allrs879255408
SNP Nexus

SNPshotrs879255408
SNPdbers879255408
MSV3drs879255408
GWAS Ctlgrs879255408
Max Magnitude0
ClinVar
Risk rs879255408(T;T)
Alt rs879255408(T;T)
Reference rs879255408(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LARS2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.45561759C>T
CLNSRC
CLNACC RCV000239073.1,