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rs1060502086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502086(G;T)
Make rs1060502086(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position11039554
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1060502086
dbSNP (old)rs1060502086
ClinGenrs1060502086
ebirs1060502086
HLIrs1060502086
Exacrs1060502086
Gnomadrs1060502086
Varsomers1060502086
Maprs1060502086
PheGenIrs1060502086
Biobankrs1060502086
1000 genomesrs1060502086
hgdprs1060502086
ensemblrs1060502086
gopubmedrs1060502086
geneviewrs1060502086
scholarrs1060502086
googlers1060502086
pharmgkbrs1060502086
gwascentralrs1060502086
openSNPrs1060502086
23andMers1060502086
23andMe allrs1060502086
SNPshotrs1060502086
SNPdbers1060502086
MSV3drs1060502086
GWAS Ctlgrs1060502086
Max Magnitude0
ClinVar
Risk rs1060502086(T;T)
Alt rs1060502086(T;T)
Reference Rs1060502086(G;G)
Significance Probable-Pathogenic
Disease Rhabdoid tumor predisposition syndrome 2
Variation info
Gene SMARCA4
CLNDBN Rhabdoid tumor predisposition syndrome 2
Reversed 0
HGVS NC_000019.9:g.11150230G>T
CLNSRC
CLNACC RCV000475202.1,