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rs1064796885

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome19
Position11033384
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1064796885
dbSNP (old)rs1064796885
ClinGenrs1064796885
ebirs1064796885
HLIrs1064796885
Exacrs1064796885
Gnomadrs1064796885
Varsomers1064796885
Maprs1064796885
PheGenIrs1064796885
Biobankrs1064796885
1000 genomesrs1064796885
hgdprs1064796885
ensemblrs1064796885
gopubmedrs1064796885
geneviewrs1064796885
scholarrs1064796885
googlers1064796885
pharmgkbrs1064796885
gwascentralrs1064796885
openSNPrs1064796885
23andMers1064796885
23andMe allrs1064796885
SNPshotrs1064796885
SNPdbers1064796885
MSV3drs1064796885
GWAS Ctlgrs1064796885
Max Magnitude0
ClinVar
Risk rs1064796885(C;C)
Alt rs1064796885(C;C)
Reference Rs1064796885(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCA4
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.11144060T>C
CLNSRC
CLNACC RCV000486485.1,