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rs796052053

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052053(A;G)
Make rs796052053(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position84459230
GeneDNAH6, SUCLG1
is asnp
is mentioned by
dbSNPrs796052053
ebirs796052053
HLIrs796052053
Exacrs796052053
Varsomers796052053
Maprs796052053
PheGenIrs796052053
hapmaprs796052053
1000 genomesrs796052053
hgdprs796052053
ensemblrs796052053
gopubmedrs796052053
geneviewrs796052053
scholarrs796052053
googlers796052053
pharmgkbrs796052053
gwascentralrs796052053
openSNPrs796052053
23andMers796052053
23andMe allrs796052053
SNP Nexus

SNPshotrs796052053
SNPdbers796052053
MSV3drs796052053
GWAS Ctlgrs796052053
Max Magnitude0
ClinVar
Risk rs796052053(G;G)
Alt rs796052053(G;G)
Reference rs796052053(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUCLG1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.84686354T>C
CLNSRC
CLNACC RCV000186203.2,