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rs1057517953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517953(G;T)
Make rs1057517953(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94406295
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs1057517953
dbSNP (old)rs1057517953
ClinGenrs1057517953
ebirs1057517953
HLIrs1057517953
Exacrs1057517953
Gnomadrs1057517953
Varsomers1057517953
Maprs1057517953
PheGenIrs1057517953
Biobankrs1057517953
1000 genomesrs1057517953
hgdprs1057517953
ensemblrs1057517953
gopubmedrs1057517953
geneviewrs1057517953
scholarrs1057517953
googlers1057517953
pharmgkbrs1057517953
gwascentralrs1057517953
openSNPrs1057517953
23andMers1057517953
23andMe allrs1057517953
SNPshotrs1057517953
SNPdbers1057517953
MSV3drs1057517953
GWAS Ctlgrs1057517953
Max Magnitude0
ClinVar
Risk rs1057517953(T;T)
Alt rs1057517953(T;T)
Reference Rs1057517953(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94035607G>T
CLNSRC
CLNACC RCV000414693.1,