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rs1057521068

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521068(A;A)
Make rs1057521068(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position45432008
GeneRUNX2
is asnp
is mentioned by
dbSNPrs1057521068
dbSNP (old)rs1057521068
ClinGenrs1057521068
ebirs1057521068
HLIrs1057521068
Exacrs1057521068
Gnomadrs1057521068
Varsomers1057521068
Maprs1057521068
PheGenIrs1057521068
Biobankrs1057521068
1000 genomesrs1057521068
hgdprs1057521068
ensemblrs1057521068
gopubmedrs1057521068
geneviewrs1057521068
scholarrs1057521068
googlers1057521068
pharmgkbrs1057521068
gwascentralrs1057521068
openSNPrs1057521068
23andMers1057521068
23andMe allrs1057521068
SNPshotrs1057521068
SNPdbers1057521068
MSV3drs1057521068
GWAS Ctlgrs1057521068
Max Magnitude0
ClinVar
Risk rs1057521068(A;A)
Alt rs1057521068(A;A)
Reference Rs1057521068(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RUNX2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.45399745G>A
CLNSRC
CLNACC RCV000430285.1,