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rs1057524873

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524873(G;T)
Make rs1057524873(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94421055
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs1057524873
dbSNP (old)rs1057524873
ClinGenrs1057524873
ebirs1057524873
HLIrs1057524873
Exacrs1057524873
Gnomadrs1057524873
Varsomers1057524873
Maprs1057524873
PheGenIrs1057524873
Biobankrs1057524873
1000 genomesrs1057524873
hgdprs1057524873
ensemblrs1057524873
gopubmedrs1057524873
geneviewrs1057524873
scholarrs1057524873
googlers1057524873
pharmgkbrs1057524873
gwascentralrs1057524873
openSNPrs1057524873
23andMers1057524873
23andMe allrs1057524873
SNPshotrs1057524873
SNPdbers1057524873
MSV3drs1057524873
GWAS Ctlgrs1057524873
Max Magnitude0
ClinVar
Risk rs1057524873(T;T)
Alt rs1057524873(T;T)
Reference Rs1057524873(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94050367G>T
CLNSRC
CLNACC RCV000420048.1,