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rs794728039

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728039(A;A)
Make rs794728039(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position188991047
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs794728039
ebirs794728039
HLIrs794728039
Exacrs794728039
Varsomers794728039
Maprs794728039
PheGenIrs794728039
hapmaprs794728039
1000 genomesrs794728039
hgdprs794728039
ensemblrs794728039
gopubmedrs794728039
geneviewrs794728039
scholarrs794728039
googlers794728039
pharmgkbrs794728039
gwascentralrs794728039
openSNPrs794728039
23andMers794728039
23andMe allrs794728039
SNP Nexus

SNPshotrs794728039
SNPdbers794728039
MSV3drs794728039
GWAS Ctlgrs794728039
Max Magnitude0
ClinVar
Risk rs794728039(A;A)
Alt rs794728039(A;A)
Reference rs794728039(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL3A1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189855773C>A
CLNSRC
CLNACC RCV000181074.2,