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rs1060502085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502085(-;-)
Make rs1060502085(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position10986495
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1060502085
dbSNP (old)rs1060502085
ClinGenrs1060502085
ebirs1060502085
HLIrs1060502085
Exacrs1060502085
Gnomadrs1060502085
Varsomers1060502085
Maprs1060502085
PheGenIrs1060502085
Biobankrs1060502085
1000 genomesrs1060502085
hgdprs1060502085
ensemblrs1060502085
gopubmedrs1060502085
geneviewrs1060502085
scholarrs1060502085
googlers1060502085
pharmgkbrs1060502085
gwascentralrs1060502085
openSNPrs1060502085
23andMers1060502085
23andMe allrs1060502085
SNPshotrs1060502085
SNPdbers1060502085
MSV3drs1060502085
GWAS Ctlgrs1060502085
Max Magnitude0
ClinVar
Risk rs1060502085(-;-)
Alt rs1060502085(-;-)
Reference Rs1060502085(C;C)
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.11097171delC
CLNSRC
CLNACC RCV000471726.1,