Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060502102

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502102(A;A)
Make rs1060502102(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position11023517
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1060502102
dbSNP (old)rs1060502102
ClinGenrs1060502102
ebirs1060502102
HLIrs1060502102
Exacrs1060502102
Gnomadrs1060502102
Varsomers1060502102
LitVarrs1060502102
Maprs1060502102
PheGenIrs1060502102
Biobankrs1060502102
1000 genomesrs1060502102
hgdprs1060502102
ensemblrs1060502102
gopubmedrs1060502102
geneviewrs1060502102
scholarrs1060502102
googlers1060502102
pharmgkbrs1060502102
gwascentralrs1060502102
openSNPrs1060502102
23andMers1060502102
23andMe allrs1060502102
SNPshotrs1060502102
SNPdbers1060502102
MSV3drs1060502102
GWAS Ctlgrs1060502102
Max Magnitude0
ClinVar
Risk rs1060502102(A;A)
Alt rs1060502102(A;A)
Reference Rs1060502102(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.11134193G>A
CLNSRC
CLNACC RCV000466062.1,