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rs1064795105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome19
Position11013112
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1064795105
dbSNP (classic)rs1064795105
ClinGenrs1064795105
ebirs1064795105
HLIrs1064795105
Exacrs1064795105
Gnomadrs1064795105
Varsomers1064795105
LitVarrs1064795105
Maprs1064795105
PheGenIrs1064795105
Biobankrs1064795105
1000 genomesrs1064795105
hgdprs1064795105
ensemblrs1064795105
geneviewrs1064795105
scholarrs1064795105
googlers1064795105
pharmgkbrs1064795105
gwascentralrs1064795105
openSNPrs1064795105
23andMers1064795105
23andMe allrs1064795105
SNPshotrs1064795105
SNPdbers1064795105
MSV3drs1064795105
GWAS Ctlgrs1064795105
Max Magnitude0
ClinVar
Risk rs1064795105(T;T)
Alt rs1064795105(T;T)
Reference Rs1064795105(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCA4
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.11123788C>T
CLNSRC
CLNACC RCV000478796.1,