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rs1057518136

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518136(-;-)
Make rs1057518136(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94404861
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs1057518136
dbSNP (old)rs1057518136
ClinGenrs1057518136
ebirs1057518136
HLIrs1057518136
Exacrs1057518136
Gnomadrs1057518136
Varsomers1057518136
Maprs1057518136
PheGenIrs1057518136
Biobankrs1057518136
1000 genomesrs1057518136
hgdprs1057518136
ensemblrs1057518136
gopubmedrs1057518136
geneviewrs1057518136
scholarrs1057518136
googlers1057518136
pharmgkbrs1057518136
gwascentralrs1057518136
openSNPrs1057518136
23andMers1057518136
23andMe allrs1057518136
SNPshotrs1057518136
SNPdbers1057518136
MSV3drs1057518136
GWAS Ctlgrs1057518136
Max Magnitude0
ClinVar
Risk rs1057518136(-;-)
Alt rs1057518136(-;-)
Reference Rs1057518136(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94034173delC
CLNSRC
CLNACC RCV000412781.1,