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rs794728051

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728051(A;A)
Make rs794728051(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189002973
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs794728051
ebirs794728051
HLIrs794728051
Exacrs794728051
Varsomers794728051
Maprs794728051
PheGenIrs794728051
hapmaprs794728051
1000 genomesrs794728051
hgdprs794728051
ensemblrs794728051
gopubmedrs794728051
geneviewrs794728051
scholarrs794728051
googlers794728051
pharmgkbrs794728051
gwascentralrs794728051
openSNPrs794728051
23andMers794728051
23andMe allrs794728051
SNP Nexus

SNPshotrs794728051
SNPdbers794728051
MSV3drs794728051
GWAS Ctlgrs794728051
Max Magnitude0
ClinVar
Risk rs794728051(A;A)
Alt rs794728051(A;A)
Reference rs794728051(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL3A1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189867699G>A
CLNSRC
CLNACC RCV000181096.2,