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rs794728057

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728057(C;T)
Make rs794728057(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189010708
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs794728057
ebirs794728057
HLIrs794728057
Exacrs794728057
Varsomers794728057
Maprs794728057
PheGenIrs794728057
hapmaprs794728057
1000 genomesrs794728057
hgdprs794728057
ensemblrs794728057
gopubmedrs794728057
geneviewrs794728057
scholarrs794728057
googlers794728057
pharmgkbrs794728057
gwascentralrs794728057
openSNPrs794728057
23andMers794728057
23andMe allrs794728057
SNP Nexus

SNPshotrs794728057
SNPdbers794728057
MSV3drs794728057
GWAS Ctlgrs794728057
Max Magnitude0
ClinVar
Risk rs794728057(T;T)
Alt rs794728057(T;T)
Reference rs794728057(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene COL3A1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189875434C>T
CLNSRC
CLNACC RCV000181116.1,