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rs794728050

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728050(A;G)
Make rs794728050(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189001534
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs794728050
ebirs794728050
HLIrs794728050
Exacrs794728050
Varsomers794728050
Maprs794728050
PheGenIrs794728050
hapmaprs794728050
1000 genomesrs794728050
hgdprs794728050
ensemblrs794728050
gopubmedrs794728050
geneviewrs794728050
scholarrs794728050
googlers794728050
pharmgkbrs794728050
gwascentralrs794728050
openSNPrs794728050
23andMers794728050
23andMe allrs794728050
SNP Nexus

SNPshotrs794728050
SNPdbers794728050
MSV3drs794728050
GWAS Ctlgrs794728050
Max Magnitude0
ClinVar
Risk rs794728050(G;G)
Alt rs794728050(G;G)
Reference rs794728050(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene COL3A1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189866260A>G
CLNSRC
CLNACC RCV000181095.1,