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rs1060499936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499936(A;A)
Make rs1060499936(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position11021959
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1060499936
dbSNP (old)rs1060499936
ClinGenrs1060499936
ebirs1060499936
HLIrs1060499936
Exacrs1060499936
Gnomadrs1060499936
Varsomers1060499936
LitVarrs1060499936
Maprs1060499936
PheGenIrs1060499936
Biobankrs1060499936
1000 genomesrs1060499936
hgdprs1060499936
ensemblrs1060499936
gopubmedrs1060499936
geneviewrs1060499936
scholarrs1060499936
googlers1060499936
pharmgkbrs1060499936
gwascentralrs1060499936
openSNPrs1060499936
23andMers1060499936
23andMe allrs1060499936
SNPshotrs1060499936
SNPdbers1060499936
MSV3drs1060499936
GWAS Ctlgrs1060499936
Max Magnitude0
ClinVar
Risk rs1060499936(A;A)
Alt rs1060499936(A;A)
Reference Rs1060499936(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene SMARCA4
CLNDBN Mental retardation, autosomal dominant 16
Reversed 0
HGVS NC_000019.9:g.11132635G>A
CLNSRC
CLNACC RCV000455885.1,