Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052051

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052051(A;A)
Make rs796052051(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position84431557
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs796052051
ebirs796052051
HLIrs796052051
Exacrs796052051
Varsomers796052051
Maprs796052051
PheGenIrs796052051
hapmaprs796052051
1000 genomesrs796052051
hgdprs796052051
ensemblrs796052051
gopubmedrs796052051
geneviewrs796052051
scholarrs796052051
googlers796052051
pharmgkbrs796052051
gwascentralrs796052051
openSNPrs796052051
23andMers796052051
23andMe allrs796052051
SNP Nexus

SNPshotrs796052051
SNPdbers796052051
MSV3drs796052051
GWAS Ctlgrs796052051
Max Magnitude0
ClinVar
Risk rs796052051(A;A)
Alt rs796052051(A;A)
Reference rs796052051(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLG1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.84658681C>T
CLNSRC
CLNACC RCV000186199.1,