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rs794727669

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727669(G;T)
Make rs794727669(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position94425136
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs794727669
ebirs794727669
HLIrs794727669
Exacrs794727669
Varsomers794727669
Maprs794727669
PheGenIrs794727669
hapmaprs794727669
1000 genomesrs794727669
hgdprs794727669
ensemblrs794727669
gopubmedrs794727669
geneviewrs794727669
scholarrs794727669
googlers794727669
pharmgkbrs794727669
gwascentralrs794727669
openSNPrs794727669
23andMers794727669
23andMe allrs794727669
SNP Nexus

SNPshotrs794727669
SNPdbers794727669
MSV3drs794727669
GWAS Ctlgrs794727669
Max Magnitude0
ClinVar
Risk rs794727669(T;T)
Alt rs794727669(T;T)
Reference rs794727669(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94054448G>T
CLNSRC
CLNACC RCV000178479.1,