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rs1057521663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521663(A;G)
Make rs1057521663(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position110581937
GeneSMC3
is asnp
is mentioned by
dbSNPrs1057521663
dbSNP (classic)rs1057521663
ClinGenrs1057521663
ebirs1057521663
HLIrs1057521663
Exacrs1057521663
Gnomadrs1057521663
Varsomers1057521663
LitVarrs1057521663
Maprs1057521663
PheGenIrs1057521663
Biobankrs1057521663
1000 genomesrs1057521663
hgdprs1057521663
ensemblrs1057521663
geneviewrs1057521663
scholarrs1057521663
googlers1057521663
pharmgkbrs1057521663
gwascentralrs1057521663
openSNPrs1057521663
23andMers1057521663
23andMe allrs1057521663
SNPshotrs1057521663
SNPdbers1057521663
MSV3drs1057521663
GWAS Ctlgrs1057521663
Max Magnitude0
ClinVar
Risk rs1057521663(G;G)
Alt rs1057521663(G;G)
Reference Rs1057521663(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMC3
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112341695A>G
CLNSRC
CLNACC RCV000443224.1,