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rs797045987

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045987(-;-)
Make rs797045987(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11059784
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs797045987
dbSNP (old)rs797045987
ClinGenrs797045987
ebirs797045987
HLIrs797045987
Exacrs797045987
Gnomadrs797045987
Varsomers797045987
Maprs797045987
PheGenIrs797045987
Biobankrs797045987
1000 genomesrs797045987
hgdprs797045987
ensemblrs797045987
gopubmedrs797045987
geneviewrs797045987
scholarrs797045987
googlers797045987
pharmgkbrs797045987
gwascentralrs797045987
openSNPrs797045987
23andMers797045987
23andMe allrs797045987
SNP Nexus

SNPshotrs797045987
SNPdbers797045987
MSV3drs797045987
GWAS Ctlgrs797045987
Max Magnitude0
ClinVar
Risk rs797045987(-;-)
Alt rs797045987(-;-)
Reference Rs797045987(T;T)
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.11170460delT
CLNSRC
CLNACC RCV000194866.1,