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rs796052042

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052042(A;A)
Make rs796052042(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position48898734
GeneSLC25A20
is asnp
is mentioned by
dbSNPrs796052042
ebirs796052042
HLIrs796052042
Exacrs796052042
Varsomers796052042
Maprs796052042
PheGenIrs796052042
hapmaprs796052042
1000 genomesrs796052042
hgdprs796052042
ensemblrs796052042
gopubmedrs796052042
geneviewrs796052042
scholarrs796052042
googlers796052042
pharmgkbrs796052042
gwascentralrs796052042
openSNPrs796052042
23andMers796052042
23andMe allrs796052042
SNP Nexus

SNPshotrs796052042
SNPdbers796052042
MSV3drs796052042
GWAS Ctlgrs796052042
Max Magnitude0
ClinVar
Risk rs796052042(A;A)
Alt rs796052042(A;A)
Reference rs796052042(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC25A20
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.48936167C>T
CLNSRC
CLNACC RCV000186167.1,