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rs794728054

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728054(A;A)
Make rs794728054(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189004009
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs794728054
ebirs794728054
HLIrs794728054
Exacrs794728054
Varsomers794728054
Maprs794728054
PheGenIrs794728054
hapmaprs794728054
1000 genomesrs794728054
hgdprs794728054
ensemblrs794728054
gopubmedrs794728054
geneviewrs794728054
scholarrs794728054
googlers794728054
pharmgkbrs794728054
gwascentralrs794728054
openSNPrs794728054
23andMers794728054
23andMe allrs794728054
SNP Nexus

SNPshotrs794728054
SNPdbers794728054
MSV3drs794728054
GWAS Ctlgrs794728054
Max Magnitude0
ClinVar
Risk rs794728054(A;A)
Alt rs794728054(A;A)
Reference rs794728054(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL3A1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189868735G>A
CLNSRC
CLNACC RCV000181101.2,