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

rs1060502088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502088(-;-)
Make rs1060502088(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position11039495
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1060502088
dbSNP (old)rs1060502088
ClinGenrs1060502088
ebirs1060502088
HLIrs1060502088
Exacrs1060502088
Gnomadrs1060502088
Varsomers1060502088
Maprs1060502088
PheGenIrs1060502088
Biobankrs1060502088
1000 genomesrs1060502088
hgdprs1060502088
ensemblrs1060502088
gopubmedrs1060502088
geneviewrs1060502088
scholarrs1060502088
googlers1060502088
pharmgkbrs1060502088
gwascentralrs1060502088
openSNPrs1060502088
23andMers1060502088
23andMe allrs1060502088
SNPshotrs1060502088
SNPdbers1060502088
MSV3drs1060502088
GWAS Ctlgrs1060502088
Max Magnitude0
ClinVar
Risk rs1060502088(-;-)
Alt rs1060502088(-;-)
Reference Rs1060502088(G;G)
Significance Pathogenic
Disease Rhabdoid tumor predisposition syndrome 2
Variation info
Gene SMARCA4
CLNDBN Rhabdoid tumor predisposition syndrome 2
Reversed 0
HGVS NC_000019.9:g.11150171delG
CLNSRC
CLNACC RCV000458006.1,