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rs797045980

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045980(-;-)
Make rs797045980(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11023580
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs797045980
dbSNP (old)rs797045980
ClinGenrs797045980
ebirs797045980
HLIrs797045980
Exacrs797045980
Gnomadrs797045980
Varsomers797045980
Maprs797045980
PheGenIrs797045980
Biobankrs797045980
1000 genomesrs797045980
hgdprs797045980
ensemblrs797045980
gopubmedrs797045980
geneviewrs797045980
scholarrs797045980
googlers797045980
pharmgkbrs797045980
gwascentralrs797045980
openSNPrs797045980
23andMers797045980
23andMe allrs797045980
SNP Nexus

SNPshotrs797045980
SNPdbers797045980
MSV3drs797045980
GWAS Ctlgrs797045980
Max Magnitude0
ClinVar
Risk rs797045980(-;-)
Alt rs797045980(-;-)
Reference Rs797045980(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.11134256delC
CLNSRC
CLNACC RCV000193167.1,