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rs796052052

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052052(C;T)
Make rs796052052(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position84425578
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs796052052
ebirs796052052
HLIrs796052052
Exacrs796052052
Varsomers796052052
Maprs796052052
PheGenIrs796052052
hapmaprs796052052
1000 genomesrs796052052
hgdprs796052052
ensemblrs796052052
gopubmedrs796052052
geneviewrs796052052
scholarrs796052052
googlers796052052
pharmgkbrs796052052
gwascentralrs796052052
openSNPrs796052052
23andMers796052052
23andMe allrs796052052
SNP Nexus

SNPshotrs796052052
SNPdbers796052052
MSV3drs796052052
GWAS Ctlgrs796052052
Max Magnitude0
ClinVar
Risk rs796052052(T;T)
Alt rs796052052(T;T)
Reference rs796052052(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLG1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.84652702G>A
CLNSRC
CLNACC RCV000186200.1,