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rs141295770

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141295770(A;A)
Make rs141295770(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position47949491
GeneSUCLA2
is asnp
is mentioned by
dbSNPrs141295770
ebirs141295770
HLIrs141295770
Exacrs141295770
Varsomers141295770
Maprs141295770
PheGenIrs141295770
hapmaprs141295770
1000 genomesrs141295770
hgdprs141295770
ensemblrs141295770
gopubmedrs141295770
geneviewrs141295770
scholarrs141295770
googlers141295770
pharmgkbrs141295770
gwascentralrs141295770
openSNPrs141295770
23andMers141295770
23andMe allrs141295770
SNP Nexus

SNPshotrs141295770
SNPdbers141295770
MSV3drs141295770
GWAS Ctlgrs141295770
Max Magnitude0
ClinVar
Risk rs141295770(A;A)
Alt rs141295770(A;A)
Reference rs141295770(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.48523626C>A
CLNSRC
CLNACC RCV000186187.1,