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rs1057521113

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521113(A;G)
Make rs1057521113(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position11027948
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1057521113
dbSNP (old)rs1057521113
ClinGenrs1057521113
ebirs1057521113
HLIrs1057521113
Exacrs1057521113
Gnomadrs1057521113
Varsomers1057521113
Maprs1057521113
PheGenIrs1057521113
Biobankrs1057521113
1000 genomesrs1057521113
hgdprs1057521113
ensemblrs1057521113
gopubmedrs1057521113
geneviewrs1057521113
scholarrs1057521113
googlers1057521113
pharmgkbrs1057521113
gwascentralrs1057521113
openSNPrs1057521113
23andMers1057521113
23andMe allrs1057521113
SNPshotrs1057521113
SNPdbers1057521113
MSV3drs1057521113
GWAS Ctlgrs1057521113
Max Magnitude0
ClinVar
Risk rs1057521113(G;G)
Alt rs1057521113(G;G)
Reference Rs1057521113(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCA4
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.11138624A>G
CLNSRC
CLNACC RCV000440122.1,