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rs1057518209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518209(C;C)
Make rs1057518209(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94423084
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs1057518209
dbSNP (old)rs1057518209
ClinGenrs1057518209
ebirs1057518209
HLIrs1057518209
Exacrs1057518209
Gnomadrs1057518209
Varsomers1057518209
LitVarrs1057518209
Maprs1057518209
PheGenIrs1057518209
Biobankrs1057518209
1000 genomesrs1057518209
hgdprs1057518209
ensemblrs1057518209
gopubmedrs1057518209
geneviewrs1057518209
scholarrs1057518209
googlers1057518209
pharmgkbrs1057518209
gwascentralrs1057518209
openSNPrs1057518209
23andMers1057518209
23andMe allrs1057518209
SNPshotrs1057518209
SNPdbers1057518209
MSV3drs1057518209
GWAS Ctlgrs1057518209
Max Magnitude0
ClinVar
Risk rs1057518209(C;C)
Alt rs1057518209(C;C)
Reference Rs1057518209(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94052396G>C
CLNSRC
CLNACC RCV000414112.1,