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rs796052045

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052045(C;C)
Make rs796052045(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position47954405
GeneSUCLA2
is asnp
is mentioned by
dbSNPrs796052045
ebirs796052045
HLIrs796052045
Exacrs796052045
Varsomers796052045
Maprs796052045
PheGenIrs796052045
hapmaprs796052045
1000 genomesrs796052045
hgdprs796052045
ensemblrs796052045
gopubmedrs796052045
geneviewrs796052045
scholarrs796052045
googlers796052045
pharmgkbrs796052045
gwascentralrs796052045
openSNPrs796052045
23andMers796052045
23andMe allrs796052045
SNP Nexus

SNPshotrs796052045
SNPdbers796052045
MSV3drs796052045
GWAS Ctlgrs796052045
Max Magnitude0
ClinVar
Risk rs796052045(C;C)
Alt rs796052045(C;C)
Reference rs796052045(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLA2
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.48528540C>G
CLNSRC
CLNACC RCV000186183.2,