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rs786205560

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205560(A;C)
Make rs786205560(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position45419670
GeneLARS2
is asnp
is mentioned by
dbSNPrs786205560
ebirs786205560
HLIrs786205560
Exacrs786205560
Varsomers786205560
Maprs786205560
PheGenIrs786205560
hapmaprs786205560
1000 genomesrs786205560
hgdprs786205560
ensemblrs786205560
gopubmedrs786205560
geneviewrs786205560
scholarrs786205560
googlers786205560
pharmgkbrs786205560
gwascentralrs786205560
openSNPrs786205560
23andMers786205560
23andMe allrs786205560
SNP Nexus

SNPshotrs786205560
SNPdbers786205560
MSV3drs786205560
GWAS Ctlgrs786205560
Max Magnitude0
ClinVar
Risk rs786205560(C;C)
Alt rs786205560(C;C)
Reference rs786205560(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LARS2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.45461162A>C
CLNSRC
CLNACC RCV000171359.1,