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rs794728038

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728038(C;C)
Make rs794728038(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position188987144
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs794728038
ebirs794728038
HLIrs794728038
Exacrs794728038
Varsomers794728038
Maprs794728038
PheGenIrs794728038
hapmaprs794728038
1000 genomesrs794728038
hgdprs794728038
ensemblrs794728038
gopubmedrs794728038
geneviewrs794728038
scholarrs794728038
googlers794728038
pharmgkbrs794728038
gwascentralrs794728038
openSNPrs794728038
23andMers794728038
23andMe allrs794728038
SNP Nexus

SNPshotrs794728038
SNPdbers794728038
MSV3drs794728038
GWAS Ctlgrs794728038
Max Magnitude0
ClinVar
Risk rs794728038(C;C)
Alt rs794728038(C;C)
Reference rs794728038(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL3A1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189851870G>C
CLNSRC
CLNACC RCV000181068.1,