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rs796052050

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052050(A;C)
Make rs796052050(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position84443364
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs796052050
ebirs796052050
HLIrs796052050
Exacrs796052050
Varsomers796052050
Maprs796052050
PheGenIrs796052050
hapmaprs796052050
1000 genomesrs796052050
hgdprs796052050
ensemblrs796052050
gopubmedrs796052050
geneviewrs796052050
scholarrs796052050
googlers796052050
pharmgkbrs796052050
gwascentralrs796052050
openSNPrs796052050
23andMers796052050
23andMe allrs796052050
SNP Nexus

SNPshotrs796052050
SNPdbers796052050
MSV3drs796052050
GWAS Ctlgrs796052050
Max Magnitude0
ClinVar
Risk rs796052050(C;C)
Alt rs796052050(C;C)
Reference rs796052050(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLG1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.84670488T>G
CLNSRC
CLNACC RCV000186197.2,