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rs1057524847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524847(A;A)
Make rs1057524847(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94404867
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs1057524847
dbSNP (classic)rs1057524847
ClinGenrs1057524847
ebirs1057524847
HLIrs1057524847
Exacrs1057524847
Gnomadrs1057524847
Varsomers1057524847
LitVarrs1057524847
Maprs1057524847
PheGenIrs1057524847
Biobankrs1057524847
1000 genomesrs1057524847
hgdprs1057524847
ensemblrs1057524847
geneviewrs1057524847
scholarrs1057524847
googlers1057524847
pharmgkbrs1057524847
gwascentralrs1057524847
openSNPrs1057524847
23andMers1057524847
23andMe allrs1057524847
SNPshotrs1057524847
SNPdbers1057524847
MSV3drs1057524847
GWAS Ctlgrs1057524847
Max Magnitude0
ClinVar
Risk rs1057524847(A;A)
Alt rs1057524847(A;A)
Reference Rs1057524847(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94034179G>A
CLNSRC
CLNACC RCV000430596.1,