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rs796052049

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052049(C;T)
Make rs796052049(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position84441450
GeneSUCLG1
is asnp
is mentioned by
dbSNPrs796052049
ebirs796052049
HLIrs796052049
Exacrs796052049
Varsomers796052049
Maprs796052049
PheGenIrs796052049
hapmaprs796052049
1000 genomesrs796052049
hgdprs796052049
ensemblrs796052049
gopubmedrs796052049
geneviewrs796052049
scholarrs796052049
googlers796052049
pharmgkbrs796052049
gwascentralrs796052049
openSNPrs796052049
23andMers796052049
23andMe allrs796052049
SNP Nexus

SNPshotrs796052049
SNPdbers796052049
MSV3drs796052049
GWAS Ctlgrs796052049
Max Magnitude0
ClinVar
Risk rs796052049(T;T)
Alt rs796052049(T;T)
Reference rs796052049(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SUCLG1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.84668574G>A
CLNSRC
CLNACC RCV000186196.1,