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rs1057518166

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518166(C;T)
Make rs1057518166(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position40631657
GeneSMARCE1
is asnp
is mentioned by
dbSNPrs1057518166
dbSNP (old)rs1057518166
ClinGenrs1057518166
ebirs1057518166
HLIrs1057518166
Exacrs1057518166
Gnomadrs1057518166
Varsomers1057518166
Maprs1057518166
PheGenIrs1057518166
Biobankrs1057518166
1000 genomesrs1057518166
hgdprs1057518166
ensemblrs1057518166
gopubmedrs1057518166
geneviewrs1057518166
scholarrs1057518166
googlers1057518166
pharmgkbrs1057518166
gwascentralrs1057518166
openSNPrs1057518166
23andMers1057518166
23andMe allrs1057518166
SNPshotrs1057518166
SNPdbers1057518166
MSV3drs1057518166
GWAS Ctlgrs1057518166
Max Magnitude0
ClinVar
Risk rs1057518166(T;T)
Alt rs1057518166(T;T)
Reference Rs1057518166(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SMARCE1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.38787909G>A
CLNSRC
CLNACC RCV000412917.1,